gnomAD v2:
gnomAD v3:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.107001328A>T , CM000674.2:g.107001328A>T | GRCh38 |
| NC_000012.11:g.107395106A>T , CM000674.1:g.107395106A>T | GRCh37 |
| NC_000012.10:g.105919236A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000008527.10:c.636T>A MANE Select | ENSP00000008527.5:p.Gly212= | |
| ENST00000008527.9:c.636T>A | ENSP00000008527.5:p.Gly212= | |
| ENST00000546722.1:n.129T>A | ||
| ENST00000552790.5:n.1195T>A | ||
| NM_004075.4:c.636T>A | NP_004066.1:p.Gly212= | |
| XM_011537939.1:c.552T>A | XP_011536241.1:p.Gly184= | |
| XM_017018832.2:c.552T>A | XP_016874321.1:p.Gly184= | |
| XM_024448844.1:c.636T>A | XP_024304612.1:p.Gly212= | |
| XM_024448845.1:c.552T>A | XP_024304613.1:p.Gly184= | |
| NM_004075.5:c.636T>A MANE Select | NP_004066.1:p.Gly212= |