Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130872038T= , CM000671.2:g.130872038T= | GRCh38 |
| NC_000009.11:g.133747425T= , CM000671.1:g.133747425T= | GRCh37 |
| NC_000009.10:g.132737246T= | NCBI36 |
| NG_012034.1:g.163158T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372348.9:c.880-91T= | ENSP00000361423.2:n.880-91T= | |
| ENST00000318560.6:c.823-91T= MANE Select | ENSP00000323315.5:n.823-91T= | |
| ENST00000372348.7:c.880-91T= | ENSP00000361423.2:n.880-91T= | |
| ENST00000318560.5:c.823-91T= | ENSP00000323315.5:n.823-91T= | |
| ENST00000372348.6:c.880-91T= | ENSP00000361423.2:n.880-91T= | |
| NM_005157.5:c.823-91T= | NP_005148.2:n.823-91T= | |
| NM_007313.2:c.880-91T= | NP_009297.2:n.880-91T= | |
| NM_005157.6:c.823-91T= MANE Select | NP_005148.2:n.823-91T= | |
| NM_007313.3:c.880-91T= | NP_009297.2:n.880-91T= |