Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73343532G>A , CM000677.2:g.73343532G>A | GRCh38 |
| NC_000015.9:g.73635873G>A , CM000677.1:g.73635873G>A | GRCh37 |
| NC_000015.8:g.71422926G>A | NCBI36 |
| NG_009063.1:g.30733C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005477.3:c.1062C>T MANE Select | NP_005468.1:p.Tyr354= |
| ENST00000261917.4:c.1062C>T MANE Select | ENSP00000261917.3:p.Tyr354= |
| NM_005477.2:c.1062C>T | NP_005468.1:p.Tyr354= |
| ENST00000261917.3:c.1062C>T | ENSP00000261917.3:p.Tyr354= |