Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1404433C= , CM000667.2:g.1404433C= | GRCh38 |
| NC_000005.9:g.1404548C= , CM000667.1:g.1404548C= | GRCh37 |
| NC_000005.8:g.1457548C= | NCBI36 |
| NG_015885.1:g.45996G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001044.5:c.1600-1344G= MANE Select | NP_001035.1:n.1600-1344G= |
| ENST00000270349.12:c.1600-1344G= MANE Select | ENSP00000270349.9:n.1600-1344G= |
| NM_001044.4:c.1600-1344G= | NP_001035.1:n.1600-1344G= |
| ENST00000270349.11:c.1600-1344G= | ENSP00000270349.9:n.1600-1344G= |