Linked Data
ClinVar Variation Id:
194148
dbSNP Id:
rs141315921
ExAC:
6:152497676 G / C
gnomAD v2:
6-152497676-G-C
gnomAD v3:
6-152176541-G-C
gnomAD v4:
6-152176541-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152176541G>C , CM000668.2:g.152176541G>C | GRCh38 |
| NC_000006.11:g.152497676G>C , CM000668.1:g.152497676G>C | GRCh37 |
| NC_000006.10:g.152539369G>C | NCBI36 |
| NG_012855.1:g.465859C>G | |
| NG_012855.2:g.465859C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.23480C>G MANE Select | ENSP00000356224.5:p.Ala7827Gly | |
| ENST00000423061.6:c.23267C>G | ENSP00000396024.1:p.Ala7756Gly | |
| ENST00000341594.9:c.22265C>G | ENSP00000341887.6:p.Ala7422Gly | |
| ENST00000347037.9:n.159C>G | ||
| ENST00000367251.7:c.2246C>G | ENSP00000356220.3:p.Ala749Gly | |
| ENST00000367255.9:c.23480C>G | ENSP00000356224.5:p.Ala7827Gly | |
| ENST00000367256.9:n.7172C>G | ||
| ENST00000367257.8:c.1418C>G | ENSP00000356226.4:p.Ala473Gly | |
| ENST00000409694.6:n.7064C>G | ||
| ENST00000423061.5:c.23267C>G | ENSP00000396024.1:p.Ala7756Gly | |
| ENST00000536990.5:n.317C>G | ||
| NM_033071.3:c.23267C>G | NP_149062.1:p.Ala7756Gly | |
| NM_182961.3:c.23480C>G | NP_892006.3:p.Ala7827Gly | |
| XM_006715407.1:c.23516C>G | XP_006715470.1:p.Ala7839Gly | |
| XM_006715408.1:c.23504C>G | XP_006715471.1:p.Ala7835Gly | |
| XM_006715409.1:c.23495C>G | XP_006715472.1:p.Ala7832Gly | |
| XM_006715410.1:c.23516C>G | XP_006715473.1:p.Ala7839Gly | |
| XM_006715411.1:c.23465C>G | XP_006715474.1:p.Ala7822Gly | |
| XM_006715412.1:c.23501C>G | XP_006715475.1:p.Ala7834Gly | |
| XM_006715413.1:c.23516C>G | XP_006715476.1:p.Ala7839Gly | |
| XM_006715414.1:c.23444C>G | XP_006715477.1:p.Ala7815Gly | |
| XM_006715415.1:c.23516C>G | XP_006715478.1:p.Ala7839Gly | |
| XM_006715416.1:c.23501C>G | XP_006715479.1:p.Ala7834Gly | |
| XM_006715417.1:c.23375C>G | XP_006715480.1:p.Ala7792Gly | |
| XM_006715420.1:c.23363C>G | XP_006715483.1:p.Ala7788Gly | |
| XM_006715421.1:c.23360C>G | XP_006715484.1:p.Ala7787Gly | |
| XM_006715422.1:c.23357C>G | XP_006715485.1:p.Ala7786Gly | |
| XM_006715423.1:c.23516C>G | XP_006715486.1:p.Ala7839Gly | |
| XM_006715424.1:c.23516C>G | XP_006715487.1:p.Ala7839Gly | |
| XM_006715425.1:c.23516C>G | XP_006715488.1:p.Ala7839Gly | |
| XM_011535641.1:c.23513C>G | XP_011533943.1:p.Ala7838Gly | |
| XM_011535642.1:c.23501C>G | XP_011533944.1:p.Ala7834Gly | |
| XM_011535643.1:c.23351C>G | XP_011533945.1:p.Ala7784Gly | |
| XM_011535644.1:c.21791C>G | XP_011533946.1:p.Ala7264Gly | |
| XM_011535645.1:c.21284C>G | XP_011533947.1:p.Ala7095Gly | |
| XM_011535647.1:c.16751C>G | XP_011533949.1:p.Ala5584Gly | |
| NM_001347701.1:c.86C>G | NP_001334630.1:p.Ala29Gly | |
| XM_006715408.2:c.23504C>G | XP_006715471.1:p.Ala7835Gly | |
| XM_006715410.2:c.23516C>G | XP_006715473.1:p.Ala7839Gly | |
| XM_006715412.2:c.23501C>G | XP_006715475.1:p.Ala7834Gly | |
| XM_006715413.2:c.23516C>G | XP_006715476.1:p.Ala7839Gly | |
| XM_006715415.2:c.23516C>G | XP_006715478.1:p.Ala7839Gly | |
| XM_006715416.2:c.23501C>G | XP_006715479.1:p.Ala7834Gly | |
| XM_006715417.2:c.23375C>G | XP_006715480.1:p.Ala7792Gly | |
| XM_006715420.2:c.23363C>G | XP_006715483.1:p.Ala7788Gly | |
| XM_006715421.2:c.23360C>G | XP_006715484.1:p.Ala7787Gly | |
| XM_006715423.2:c.23516C>G | XP_006715486.1:p.Ala7839Gly | |
| XM_006715424.2:c.23516C>G | XP_006715487.1:p.Ala7839Gly | |
| XM_006715425.2:c.23516C>G | XP_006715488.1:p.Ala7839Gly | |
| XM_011535641.2:c.23513C>G | XP_011533943.1:p.Ala7838Gly | |
| XM_011535642.2:c.23501C>G | XP_011533944.1:p.Ala7834Gly | |
| XM_011535645.2:c.21284C>G | XP_011533947.1:p.Ala7095Gly | |
| XM_017010608.1:c.23516C>G | XP_016866097.1:p.Ala7839Gly | |
| XM_017010609.1:c.23516C>G | XP_016866098.1:p.Ala7839Gly | |
| XM_017010610.1:c.23495C>G | XP_016866099.1:p.Ala7832Gly | |
| XM_017010611.2:c.23489C>G | XP_016866100.1:p.Ala7830Gly | |
| XM_017010612.1:c.23438C>G | XP_016866101.1:p.Ala7813Gly | |
| XM_017010613.1:c.23513C>G | XP_016866102.1:p.Ala7838Gly | |
| XM_017010614.1:c.23360C>G | XP_016866103.1:p.Ala7787Gly | |
| XM_017010615.1:c.23360C>G | XP_016866104.1:p.Ala7787Gly | |
| XM_017010616.1:c.23516C>G | XP_016866105.1:p.Ala7839Gly | |
| XM_017010617.1:c.23513C>G | XP_016866106.1:p.Ala7838Gly | |
| XM_017010618.1:c.23501C>G | XP_016866107.1:p.Ala7834Gly | |
| XM_017010619.1:c.21791C>G | XP_016866108.1:p.Ala7264Gly | |
| NM_182961.4:c.23480C>G MANE Select | NP_892006.3:p.Ala7827Gly | |
| NM_001347701.2:c.86C>G | NP_001334630.1:p.Ala29Gly | |
| NM_033071.5:c.23267C>G | NP_149062.2:p.Ala7756Gly |