Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.172956746C>G , CM000665.2:g.172956746C>G | GRCh38 |
| NC_000003.11:g.172674536C>G , CM000665.1:g.172674536C>G | GRCh37 |
| NC_000003.10:g.174157230C>G | NCBI36 |
| NG_021422.1:g.189523G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351008.4:c.1012G>C MANE Select | ENSP00000341765.3:p.Asp338His | |
| ENST00000652082.1:c.164G>C | ||
| ENST00000351008.3:c.1012G>C | ENSP00000341765.3:p.Asp338His | |
| NM_031955.5:c.1012G>C | NP_114161.3:p.Asp338His | |
| XM_006713778.2:c.1012G>C | XP_006713841.1:p.Asp338His | |
| XM_011513222.1:c.1012G>C | XP_011511524.1:p.Asp338His | |
| XM_006713778.3:c.1012G>C | XP_006713841.1:p.Asp338His | |
| XM_017007308.2:c.1012G>C | XP_016862797.1:p.Asp338His | |
| NM_031955.6:c.1012G>C MANE Select | NP_114161.3:p.Asp338His |