Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130862971A= , CM000671.2:g.130862971A= | GRCh38 |
| NC_000009.11:g.133738358A= , CM000671.1:g.133738358A= | GRCh37 |
| NC_000009.10:g.132728179A= | NCBI36 |
| NG_012034.1:g.154091A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005157.6:c.758A= MANE Select | NP_005148.2:p.Tyr253= |
| ENST00000318560.6:c.758A= MANE Select | ENSP00000323315.5:p.Tyr253= |
| NM_005157.5:c.758A= | NP_005148.2:p.Tyr253= |
| NM_007313.2:c.815A= | NP_009297.2:p.Tyr272= |
| NM_007313.3:c.815A= | NP_009297.2:p.Tyr272= |
| ENST00000318560.5:c.758A= | ENSP00000323315.5:p.Tyr253= |
| ENST00000372348.6:c.815A= | ENSP00000361423.2:p.Tyr272= |
| ENST00000372348.7:c.815A= | ENSP00000361423.2:p.Tyr272= |
| ENST00000372348.9:c.815A= | ENSP00000361423.2:p.Tyr272= |