Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57565399C= , CM000682.2:g.57565399C= | GRCh38 |
| NC_000020.10:g.56140455C= , CM000682.1:g.56140455C= | GRCh37 |
| NC_000020.9:g.55573861C= | NCBI36 |
| NG_008205.1:g.9319C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.1464C= MANE Select | ENSP00000319814.4:p.Tyr488= | |
| ENST00000319441.5:c.1464C= | ENSP00000319814.4:p.Tyr488= | |
| ENST00000467047.1:n.4106C= | ||
| NM_002591.3:c.1464C= | NP_002582.3:p.Tyr488= | |
| XM_011528839.1:c.1068C= | XP_011527141.1:p.Tyr356= | |
| XM_024451888.1:c.1068C= | XP_024307656.1:p.Tyr356= | |
| NM_002591.4:c.1464C= MANE Select | NP_002582.3:p.Tyr488= |