Linked Data
ClinVar Variation Id:
382696
dbSNP Id:
rs1057521423
gnomAD v2:
6-152464755-T-C
gnomAD v3:
6-152143620-T-C
gnomAD v4:
6-152143620-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152143620T>C , CM000668.2:g.152143620T>C | GRCh38 |
| NC_000006.11:g.152464755T>C , CM000668.1:g.152464755T>C | GRCh37 |
| NC_000006.10:g.152506448T>C | NCBI36 |
| NG_012855.1:g.498780A>G | |
| NG_012855.2:g.498780A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.1653+3A>G MANE Plus Clinical | ENSP00000346701.4:n.1653+3A>G | |
| ENST00000367255.10:c.25119+3A>G MANE Select | ENSP00000356224.5:n.25119+3A>G | |
| ENST00000423061.6:c.24975+3A>G | ENSP00000396024.1:n.24975+3A>G | |
| ENST00000672154.1:c.521+3A>G | ||
| ENST00000672169.1:c.854+3A>G | ||
| ENST00000673173.1:c.891-3459A>G | ||
| ENST00000673451.1:c.891+3A>G | ENSP00000500189.1:n.891+3A>G | |
| ENST00000341594.9:c.23904+3A>G | ENSP00000341887.6:n.23904+3A>G | |
| ENST00000347037.9:n.1867+3A>G | ||
| ENST00000354674.4:c.1653+3A>G | ENSP00000346701.4:n.1653+3A>G | |
| ENST00000367251.7:c.3954+3A>G | ENSP00000356220.3:n.3954+3A>G | |
| ENST00000367255.9:c.25119+3A>G | ENSP00000356224.5:n.25119+3A>G | |
| ENST00000367256.9:n.8811+3A>G | ||
| ENST00000367257.8:c.3057+3A>G | ENSP00000356226.4:n.3057+3A>G | |
| ENST00000409694.6:n.8703+3A>G | ||
| ENST00000423061.5:c.24975+3A>G | ENSP00000396024.1:n.24975+3A>G | |
| ENST00000460912.6:n.1733+3A>G | ||
| ENST00000478916.5:n.4141+3A>G | ||
| ENST00000536990.5:n.1956+3A>G | ||
| ENST00000539504.5:c.1584+3A>G | ENSP00000441052.1:n.1584+3A>G | |
| NM_033071.3:c.24975+3A>G | NP_149062.1:n.24975+3A>G | |
| NM_182961.3:c.25119+3A>G | NP_892006.3:n.25119+3A>G | |
| XM_006715407.1:c.25224+3A>G | XP_006715470.1:n.25224+3A>G | |
| XM_006715408.1:c.25212+3A>G | XP_006715471.1:n.25212+3A>G | |
| XM_006715409.1:c.25203+3A>G | XP_006715472.1:n.25203+3A>G | |
| XM_006715410.1:c.25224+3A>G | XP_006715473.1:n.25224+3A>G | |
| XM_006715411.1:c.25173+3A>G | XP_006715474.1:n.25173+3A>G | |
| XM_006715412.1:c.25209+3A>G | XP_006715475.1:n.25209+3A>G | |
| XM_006715413.1:c.25155+3A>G | XP_006715476.1:n.25155+3A>G | |
| XM_006715414.1:c.25152+3A>G | XP_006715477.1:n.25152+3A>G | |
| XM_006715415.1:c.25155+3A>G | XP_006715478.1:n.25155+3A>G | |
| XM_006715416.1:c.25140+3A>G | XP_006715479.1:n.25140+3A>G | |
| XM_006715417.1:c.25083+3A>G | XP_006715480.1:n.25083+3A>G | |
| XM_006715420.1:c.25071+3A>G | XP_006715483.1:n.25071+3A>G | |
| XM_006715421.1:c.25068+3A>G | XP_006715484.1:n.25068+3A>G | |
| XM_006715422.1:c.25065+3A>G | XP_006715485.1:n.25065+3A>G | |
| XM_006715423.1:c.25224+3A>G | XP_006715486.1:n.25224+3A>G | |
| XM_006715424.1:c.25224+3A>G | XP_006715487.1:n.25224+3A>G | |
| XM_006715425.1:c.25155+3A>G | XP_006715488.1:n.25155+3A>G | |
| XM_011535641.1:c.25221+3A>G | XP_011533943.1:n.25221+3A>G | |
| XM_011535642.1:c.25209+3A>G | XP_011533944.1:n.25209+3A>G | |
| XM_011535643.1:c.25059+3A>G | XP_011533945.1:n.25059+3A>G | |
| XM_011535644.1:c.23499+3A>G | XP_011533946.1:n.23499+3A>G | |
| XM_011535645.1:c.22992+3A>G | XP_011533947.1:n.22992+3A>G | |
| XM_011535647.1:c.18459+3A>G | XP_011533949.1:n.18459+3A>G | |
| NM_001347701.1:c.1725+3A>G | NP_001334630.1:n.1725+3A>G | |
| NM_001347702.1:c.1653+3A>G | NP_001334631.1:n.1653+3A>G | |
| XM_006715408.2:c.25212+3A>G | XP_006715471.1:n.25212+3A>G | |
| XM_006715410.2:c.25224+3A>G | XP_006715473.1:n.25224+3A>G | |
| XM_006715412.2:c.25209+3A>G | XP_006715475.1:n.25209+3A>G | |
| XM_006715413.2:c.25155+3A>G | XP_006715476.1:n.25155+3A>G | |
| XM_006715415.2:c.25155+3A>G | XP_006715478.1:n.25155+3A>G | |
| XM_006715416.2:c.25140+3A>G | XP_006715479.1:n.25140+3A>G | |
| XM_006715417.2:c.25083+3A>G | XP_006715480.1:n.25083+3A>G | |
| XM_006715420.2:c.25071+3A>G | XP_006715483.1:n.25071+3A>G | |
| XM_006715421.2:c.25068+3A>G | XP_006715484.1:n.25068+3A>G | |
| XM_006715423.2:c.25224+3A>G | XP_006715486.1:n.25224+3A>G | |
| XM_006715424.2:c.25224+3A>G | XP_006715487.1:n.25224+3A>G | |
| XM_006715425.2:c.25155+3A>G | XP_006715488.1:n.25155+3A>G | |
| XM_011535641.2:c.25221+3A>G | XP_011533943.1:n.25221+3A>G | |
| XM_011535642.2:c.25209+3A>G | XP_011533944.1:n.25209+3A>G | |
| XM_011535645.2:c.22992+3A>G | XP_011533947.1:n.22992+3A>G | |
| XM_017010608.1:c.25224+3A>G | XP_016866097.1:n.25224+3A>G | |
| XM_017010609.1:c.25224+3A>G | XP_016866098.1:n.25224+3A>G | |
| XM_017010610.1:c.25203+3A>G | XP_016866099.1:n.25203+3A>G | |
| XM_017010611.2:c.25197+3A>G | XP_016866100.1:n.25197+3A>G | |
| XM_017010612.1:c.25146+3A>G | XP_016866101.1:n.25146+3A>G | |
| XM_017010613.1:c.25152+3A>G | XP_016866102.1:n.25152+3A>G | |
| XM_017010614.1:c.25068+3A>G | XP_016866103.1:n.25068+3A>G | |
| XM_017010615.1:c.24999+3A>G | XP_016866104.1:n.24999+3A>G | |
| XM_017010616.1:c.25155+3A>G | XP_016866105.1:n.25155+3A>G | |
| XM_017010617.1:c.25152+3A>G | XP_016866106.1:n.25152+3A>G | |
| XM_017010618.1:c.25140+3A>G | XP_016866107.1:n.25140+3A>G | |
| XM_017010619.1:c.23499+3A>G | XP_016866108.1:n.23499+3A>G | |
| NM_182961.4:c.25119+3A>G MANE Select | NP_892006.3:n.25119+3A>G | |
| NM_001347701.2:c.1725+3A>G | NP_001334630.1:n.1725+3A>G | |
| NM_001347702.2:c.1653+3A>G MANE Plus Clinical | NP_001334631.1:n.1653+3A>G | |
| NM_033071.5:c.24975+3A>G | NP_149062.2:n.24975+3A>G |