Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57565426G= , CM000682.2:g.57565426G= | GRCh38 |
| NC_000020.10:g.56140482G= , CM000682.1:g.56140482G= | GRCh37 |
| NC_000020.9:g.55573888G= | NCBI36 |
| NG_008205.1:g.9346G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.1491G= MANE Select | ENSP00000319814.4:p.Trp497= | |
| ENST00000319441.5:c.1491G= | ENSP00000319814.4:p.Trp497= | |
| ENST00000467047.1:n.4133G= | ||
| NM_002591.3:c.1491G= | NP_002582.3:p.Trp497= | |
| XM_011528839.1:c.1095G= | XP_011527141.1:p.Trp365= | |
| XM_024451888.1:c.1095G= | XP_024307656.1:p.Trp365= | |
| NM_002591.4:c.1491G= MANE Select | NP_002582.3:p.Trp497= |