Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73442367A= , CM000666.2:g.73442367A= | GRCh38 |
| NC_000004.11:g.74308084A= , CM000666.1:g.74308084A= | GRCh37 |
| NC_000004.10:g.74526948A= | NCBI36 |
| NG_023028.1:g.11152A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395792.7:c.554A= MANE Select | ENSP00000379138.2:p.Tyr185= | |
| ENST00000226359.2:c.554A= | ENSP00000226359.2:p.Tyr185= | |
| ENST00000395792.6:c.554A= | ENSP00000379138.2:p.Tyr185= | |
| NM_001134.2:c.554A= | NP_001125.1:p.Tyr185= | |
| XM_011531704.1:c.551A= | XP_011530006.1:p.Tyr184= | |
| NM_001354717.1:c.80A= | NP_001341646.1:p.Tyr27= | |
| NM_001134.3:c.554A= MANE Select | NP_001125.1:p.Tyr185= | |
| NM_001354717.2:c.80A= | NP_001341646.2:p.Tyr27= |