Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39503026C>A , CM000681.2:g.39503026C>A | GRCh38 |
| NC_000019.9:g.39993666C>A , CM000681.1:g.39993666C>A | GRCh37 |
| NC_000019.8:g.44685506C>A | NCBI36 |
| NG_008256.1:g.9110C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356433.10:c.621C>A MANE Select | ENSP00000348810.4:p.Cys207Ter | |
| ENST00000205143.4:c.621C>A | ENSP00000205143.3:p.Cys207Ter | |
| ENST00000356433.9:c.621C>A | ENSP00000348810.4:p.Cys207Ter | |
| ENST00000596614.5:c.409+2354C>A | ENSP00000471688.1:n.409+2354C>A | |
| ENST00000600437.1:n.701C>A | ||
| NM_016941.3:c.621C>A | NP_058637.1:p.Cys207Ter | |
| NM_203486.2:c.621C>A | NP_982353.1:p.Cys207Ter | |
| NM_016941.4:c.621C>A | NP_058637.1:p.Cys207Ter | |
| NM_203486.3:c.621C>A MANE Select | NP_982353.1:p.Cys207Ter |