Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1394962C= , CM000667.2:g.1394962C= | GRCh38 |
| NC_000005.9:g.1395077C= , CM000667.1:g.1395077C= | GRCh37 |
| NC_000005.8:g.1448077C= | NCBI36 |
| NG_015885.1:g.55467G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001044.5:c.1840-204G= MANE Select | NP_001035.1:n.1840-204G= |
| ENST00000270349.12:c.1840-204G= MANE Select | ENSP00000270349.9:n.1840-204G= |
| NM_001044.4:c.1840-204G= | NP_001035.1:n.1840-204G= |
| ENST00000270349.11:c.1840-204G= | ENSP00000270349.9:n.1840-204G= |
| ENST00000512002.2:n.221-204G= |