Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136220024G= , CM000671.2:g.136220024G= | GRCh38 |
| NC_000009.11:g.139111870G= , CM000671.1:g.139111870G= | GRCh37 |
| NC_000009.10:g.138251691G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358701.10:c.822-860C= MANE Select | ENSP00000351536.5:n.822-860C= | |
| ENST00000358701.9:c.822-860C= | ENSP00000351536.5:n.822-860C= | |
| ENST00000455222.1:c.124-860C= | ||
| ENST00000616829.4:c.822-860C= | ENSP00000483961.1:n.822-860C= | |
| NM_181701.3:c.822-860C= | NP_859052.3:n.822-860C= | |
| NM_181701.4:c.822-860C= MANE Select | NP_859052.3:n.822-860C= |