Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131890427C= , CM000668.2:g.131890427C= | GRCh38 |
| NC_000006.11:g.132211567C= , CM000668.1:g.132211567C= | GRCh37 |
| NC_000006.10:g.132253260C= | NCBI36 |
| NG_008206.1:g.87412C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684674.1:n.1125C= | ||
| ENST00000647893.1:c.2694C= MANE Select | ENSP00000498074.1:p.Leu898= | |
| ENST00000360971.6:c.2694C= | ENSP00000354238.2:p.Leu898= | |
| ENST00000513998.5:c.*1531C= | ENSP00000422424.1:n.*1531C= | |
| NM_006208.2:c.2694C= | NP_006199.2:p.Leu898= | |
| XM_011535896.1:c.1584C= | XP_011534198.1:p.Leu528= | |
| NM_006208.3:c.2694C= MANE Select | NP_006199.2:p.Leu898= |