Linked Data
gnomAD v4:
X-25013573-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25013573C>A , CM000685.2:g.25013573C>A | GRCh38 |
| NC_000023.10:g.25031690C>A , CM000685.1:g.25031690C>A | GRCh37 |
| NC_000023.9:g.24941611C>A | NCBI36 |
| NG_008281.1:g.7376G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.422G>T MANE Select | ENSP00000368332.4:p.Gly141Val | |
| ENST00000379044.4:c.422G>T | ENSP00000368332.4:p.Gly141Val | |
| NM_139058.2:c.422G>T | NP_620689.1:p.Gly141Val | |
| NM_139058.3:c.422G>T MANE Select | NP_620689.1:p.Gly141Val |