Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21880875C>A , CM000669.2:g.21880875C>A | GRCh38 |
| NC_000007.13:g.21920493C>A , CM000669.1:g.21920493C>A | GRCh37 |
| NC_000007.12:g.21887018C>A | NCBI36 |
| NG_012886.2:g.342661C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.12369C>A MANE Select | ENSP00000475939.1:p.Tyr4123Ter | |
| ENST00000328843.10:c.12390C>A | ENSP00000330671.7:p.Tyr4130Ter | |
| ENST00000409508.7:c.12369C>A | ENSP00000475939.1:p.Tyr4123Ter | |
| ENST00000620169.4:c.12390C>A | ENSP00000481693.1:p.Tyr4130Ter | |
| NM_001277115.1:c.12369C>A | NP_001264044.1:p.Tyr4123Ter | |
| NM_001277115.2:c.12369C>A MANE Select | NP_001264044.1:p.Tyr4123Ter |