Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39507400C>T , CM000681.2:g.39507400C>T | GRCh38 |
| NC_000019.9:g.39998040C>T , CM000681.1:g.39998040C>T | GRCh37 |
| NC_000019.8:g.44689880C>T | NCBI36 |
| NG_008256.1:g.13484C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_203486.3:c.1455C>T MANE Select | NP_982353.1:p.Pro485= |
| ENST00000356433.10:c.1455C>T MANE Select | ENSP00000348810.4:p.Pro485= |
| NM_016941.3:c.1455C>T | NP_058637.1:p.Pro485= |
| NM_016941.4:c.1455C>T | NP_058637.1:p.Pro485= |
| NM_203486.2:c.1455C>T | NP_982353.1:p.Pro485= |
| ENST00000205143.4:c.1455C>T | ENSP00000205143.3:p.Pro485= |
| ENST00000356433.9:c.1455C>T | ENSP00000348810.4:p.Pro485= |