Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24799968C= , CM000666.2:g.24799968C= | GRCh38 |
| NC_000004.11:g.24801590C= , CM000666.1:g.24801590C= | GRCh37 |
| NC_000004.10:g.24410688C= | NCBI36 |
| NG_012213.1:g.9506C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.447C= MANE Select | ENSP00000371554.3:p.Phe149= | |
| ENST00000382120.3:c.447C= | ENSP00000371554.3:p.Phe149= | |
| NM_003102.2:c.447C= | NP_003093.2:p.Phe149= | |
| XR_427488.1:n.637C= | ||
| NM_003102.3:c.447C= | NP_003093.2:p.Phe149= | |
| NM_003102.4:c.447C= MANE Select | NP_003093.2:p.Phe149= |