Linked Data
ClinVar Variation Id:
215394
ClinVar RCV Id:
RCV000197395
RCV000825499
RCV000625904
RCV001175319
RCV001789765
RCV001375186
RCV002517281
RCV003884394
RCV004530182
dbSNP Id:
rs200672755
ExAC:
4:6303542 G / A
gnomAD v2:
4-6303542-G-A
gnomAD v3:
4-6301815-G-A
gnomAD v4:
4-6301815-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6301815G>A , CM000666.2:g.6301815G>A | GRCh38 |
| NC_000004.11:g.6303542G>A , CM000666.1:g.6303542G>A | GRCh37 |
| NC_000004.10:g.6354443G>A | NCBI36 |
| NG_011700.1:g.36966G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.2056G>A | ENSP00000507852.1:p.Gly686Arg | |
| ENST00000683395.1:c.1997G>A | ||
| ENST00000684087.1:c.2020G>A | ENSP00000506978.1:p.Gly674Arg | |
| ENST00000506362.2:c.1771G>A | ENSP00000424103.2:p.Gly591Arg | |
| ENST00000673642.1:c.1679G>A | ENSP00000501242.1:n.1679G>A | |
| ENST00000673991.1:c.2056G>A | ENSP00000501033.1:p.Gly686Arg | |
| ENST00000226760.5:c.2020G>A MANE Select | ENSP00000226760.1:p.Gly674Arg | |
| ENST00000503569.5:c.2020G>A | ENSP00000423337.1:p.Gly674Arg | |
| ENST00000507765.1:n.2205G>A | ||
| NM_001145853.1:c.2020G>A | NP_001139325.1:p.Gly674Arg | |
| NM_006005.3:c.2020G>A MANE Select | NP_005996.2:p.Gly674Arg | |
| XM_017008586.1:c.2029G>A | XP_016864075.1:p.Gly677Arg |