Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130872168G= , CM000671.2:g.130872168G= | GRCh38 |
| NC_000009.11:g.133747555G= , CM000671.1:g.133747555G= | GRCh37 |
| NC_000009.10:g.132737376G= | NCBI36 |
| NG_012034.1:g.163288G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372348.9:c.919G= | ENSP00000361423.2:p.Ala307= | |
| ENST00000318560.6:c.862G= MANE Select | ENSP00000323315.5:p.Ala288= | |
| ENST00000372348.7:c.919G= | ENSP00000361423.2:p.Ala307= | |
| ENST00000318560.5:c.862G= | ENSP00000323315.5:p.Ala288= | |
| ENST00000372348.6:c.919G= | ENSP00000361423.2:p.Ala307= | |
| NM_005157.5:c.862G= | NP_005148.2:p.Ala288= | |
| NM_007313.2:c.919G= | NP_009297.2:p.Ala307= | |
| NM_005157.6:c.862G= MANE Select | NP_005148.2:p.Ala288= | |
| NM_007313.3:c.919G= | NP_009297.2:p.Ala307= |