Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.44540940G= , CM000685.2:g.44540940G= | GRCh38 |
| NC_000023.10:g.44400186G= , CM000685.1:g.44400186G= | GRCh37 |
| NC_000023.9:g.44285130G= | NCBI36 |
| NG_021288.1:g.7036C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173794.4:c.185+1005C= MANE Select | NP_776155.1:n.185+1005C= |
| ENST00000378045.5:c.185+1005C= MANE Select | ENSP00000367284.4:n.185+1005C= |
| NM_173794.3:c.185+1005C= | NP_776155.1:n.185+1005C= |
| ENST00000378045.4:c.185+1005C= | ENSP00000367284.4:n.185+1005C= |
| ENST00000483115.1:n.360+1005C= |