Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30304645G= , CM000685.2:g.30304645G= | GRCh38 |
| NC_000023.10:g.30322762G= , CM000685.1:g.30322762G= | GRCh37 |
| NC_000023.9:g.30232683G= | NCBI36 |
| NG_009814.1:g.9734C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378970.5:c.1347C= MANE Select | ENSP00000368253.4:p.Phe449= | |
| ENST00000378970.4:c.1347C= | ENSP00000368253.4:p.Phe449= | |
| NM_000475.4:c.1347C= | NP_000466.2:p.Phe449= | |
| NM_000475.5:c.1347C= MANE Select | NP_000466.2:p.Phe449= |