Linked Data
dbSNP Id:
rs778663139
ExAC:
6:152461173 C / T
gnomAD v2:
6-152461173-C-T
gnomAD v3:
6-152140038-C-T
gnomAD v4:
6-152140038-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152140038C>T , CM000668.2:g.152140038C>T | GRCh38 |
| NC_000006.11:g.152461173C>T , CM000668.1:g.152461173C>T | GRCh37 |
| NC_000006.10:g.152502866C>T | NCBI36 |
| NG_012855.1:g.502362G>A | |
| NG_012855.2:g.502362G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.1904G>A MANE Plus Clinical | ENSP00000346701.4:p.Gly635Glu | |
| ENST00000367255.10:c.25370G>A MANE Select | ENSP00000356224.5:p.Gly8457Glu | |
| ENST00000423061.6:c.25226G>A | ENSP00000396024.1:p.Gly8409Glu | |
| ENST00000672154.1:c.772G>A | ||
| ENST00000672169.1:c.1105G>A | ||
| ENST00000673173.1:c.1014G>A | ||
| ENST00000673451.1:c.1142G>A | ENSP00000500189.1:p.Gly381Glu | |
| ENST00000341594.9:c.24155G>A | ENSP00000341887.6:p.Gly8052Glu | |
| ENST00000347037.9:n.2118G>A | ||
| ENST00000354674.4:c.1904G>A | ENSP00000346701.4:p.Gly635Glu | |
| ENST00000367251.7:c.4205G>A | ENSP00000356220.3:p.Gly1402Glu | |
| ENST00000367255.9:c.25370G>A | ENSP00000356224.5:p.Gly8457Glu | |
| ENST00000367256.9:n.9062G>A | ||
| ENST00000367257.8:c.3308G>A | ENSP00000356226.4:p.Gly1103Glu | |
| ENST00000409694.6:n.8954G>A | ||
| ENST00000423061.5:c.25226G>A | ENSP00000396024.1:p.Gly8409Glu | |
| ENST00000460912.6:n.1984G>A | ||
| ENST00000478916.5:n.4392G>A | ||
| ENST00000536990.5:n.2207G>A | ||
| ENST00000539504.5:c.1835G>A | ENSP00000441052.1:p.Gly612Glu | |
| NM_033071.3:c.25226G>A | NP_149062.1:p.Gly8409Glu | |
| NM_182961.3:c.25370G>A | NP_892006.3:p.Gly8457Glu | |
| XM_006715407.1:c.25475G>A | XP_006715470.1:p.Gly8492Glu | |
| XM_006715408.1:c.25463G>A | XP_006715471.1:p.Gly8488Glu | |
| XM_006715409.1:c.25454G>A | XP_006715472.1:p.Gly8485Glu | |
| XM_006715410.1:c.25475G>A | XP_006715473.1:p.Gly8492Glu | |
| XM_006715411.1:c.25424G>A | XP_006715474.1:p.Gly8475Glu | |
| XM_006715412.1:c.25460G>A | XP_006715475.1:p.Gly8487Glu | |
| XM_006715413.1:c.25406G>A | XP_006715476.1:p.Gly8469Glu | |
| XM_006715414.1:c.25403G>A | XP_006715477.1:p.Gly8468Glu | |
| XM_006715415.1:c.25406G>A | XP_006715478.1:p.Gly8469Glu | |
| XM_006715416.1:c.25391G>A | XP_006715479.1:p.Gly8464Glu | |
| XM_006715417.1:c.25334G>A | XP_006715480.1:p.Gly8445Glu | |
| XM_006715420.1:c.25322G>A | XP_006715483.1:p.Gly8441Glu | |
| XM_006715421.1:c.25319G>A | XP_006715484.1:p.Gly8440Glu | |
| XM_006715422.1:c.25316G>A | XP_006715485.1:p.Gly8439Glu | |
| XM_006715423.1:c.25475G>A | XP_006715486.1:p.Gly8492Glu | |
| XM_006715424.1:c.25475G>A | XP_006715487.1:p.Gly8492Glu | |
| XM_006715425.1:c.25406G>A | XP_006715488.1:p.Gly8469Glu | |
| XM_011535641.1:c.25472G>A | XP_011533943.1:p.Gly8491Glu | |
| XM_011535642.1:c.25460G>A | XP_011533944.1:p.Gly8487Glu | |
| XM_011535643.1:c.25310G>A | XP_011533945.1:p.Gly8437Glu | |
| XM_011535644.1:c.23750G>A | XP_011533946.1:p.Gly7917Glu | |
| XM_011535645.1:c.23243G>A | XP_011533947.1:p.Gly7748Glu | |
| XM_011535647.1:c.18710G>A | XP_011533949.1:p.Gly6237Glu | |
| NM_001347701.1:c.1976G>A | NP_001334630.1:p.Gly659Glu | |
| NM_001347702.1:c.1904G>A | NP_001334631.1:p.Gly635Glu | |
| XM_006715408.2:c.25463G>A | XP_006715471.1:p.Gly8488Glu | |
| XM_006715410.2:c.25475G>A | XP_006715473.1:p.Gly8492Glu | |
| XM_006715412.2:c.25460G>A | XP_006715475.1:p.Gly8487Glu | |
| XM_006715413.2:c.25406G>A | XP_006715476.1:p.Gly8469Glu | |
| XM_006715415.2:c.25406G>A | XP_006715478.1:p.Gly8469Glu | |
| XM_006715416.2:c.25391G>A | XP_006715479.1:p.Gly8464Glu | |
| XM_006715417.2:c.25334G>A | XP_006715480.1:p.Gly8445Glu | |
| XM_006715420.2:c.25322G>A | XP_006715483.1:p.Gly8441Glu | |
| XM_006715421.2:c.25319G>A | XP_006715484.1:p.Gly8440Glu | |
| XM_006715423.2:c.25475G>A | XP_006715486.1:p.Gly8492Glu | |
| XM_006715424.2:c.25475G>A | XP_006715487.1:p.Gly8492Glu | |
| XM_006715425.2:c.25406G>A | XP_006715488.1:p.Gly8469Glu | |
| XM_011535641.2:c.25472G>A | XP_011533943.1:p.Gly8491Glu | |
| XM_011535642.2:c.25460G>A | XP_011533944.1:p.Gly8487Glu | |
| XM_011535645.2:c.23243G>A | XP_011533947.1:p.Gly7748Glu | |
| XM_017010608.1:c.25475G>A | XP_016866097.1:p.Gly8492Glu | |
| XM_017010609.1:c.25475G>A | XP_016866098.1:p.Gly8492Glu | |
| XM_017010610.1:c.25454G>A | XP_016866099.1:p.Gly8485Glu | |
| XM_017010611.2:c.25448G>A | XP_016866100.1:p.Gly8483Glu | |
| XM_017010612.1:c.25397G>A | XP_016866101.1:p.Gly8466Glu | |
| XM_017010613.1:c.25403G>A | XP_016866102.1:p.Gly8468Glu | |
| XM_017010614.1:c.25319G>A | XP_016866103.1:p.Gly8440Glu | |
| XM_017010615.1:c.25250G>A | XP_016866104.1:p.Gly8417Glu | |
| XM_017010616.1:c.25406G>A | XP_016866105.1:p.Gly8469Glu | |
| XM_017010617.1:c.25403G>A | XP_016866106.1:p.Gly8468Glu | |
| XM_017010618.1:c.25391G>A | XP_016866107.1:p.Gly8464Glu | |
| XM_017010619.1:c.23750G>A | XP_016866108.1:p.Gly7917Glu | |
| NM_182961.4:c.25370G>A MANE Select | NP_892006.3:p.Gly8457Glu | |
| NM_001347701.2:c.1976G>A | NP_001334630.1:p.Gly659Glu | |
| NM_001347702.2:c.1904G>A MANE Plus Clinical | NP_001334631.1:p.Gly635Glu | |
| NM_033071.5:c.25226G>A | NP_149062.2:p.Gly8409Glu |