Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562792C= , CM000682.2:g.57562792C= | GRCh38 |
| NC_000020.10:g.56137848C= , CM000682.1:g.56137848C= | GRCh37 |
| NC_000020.9:g.55571254C= | NCBI36 |
| NG_008205.1:g.6712C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.503C= MANE Select | ENSP00000319814.4:p.Ala168= | |
| ENST00000319441.5:c.503C= | ENSP00000319814.4:p.Ala168= | |
| ENST00000467047.1:n.1713C= | ||
| ENST00000498194.1:n.445C= | ||
| NM_002591.3:c.503C= | NP_002582.3:p.Ala168= | |
| XM_011528839.1:c.107C= | XP_011527141.1:p.Ala36= | |
| XM_024451888.1:c.107C= | XP_024307656.1:p.Ala36= | |
| NM_002591.4:c.503C= MANE Select | NP_002582.3:p.Ala168= |