Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.44540854A>G , CM000685.2:g.44540854A>G | GRCh38 |
| NC_000023.10:g.44400100A>G , CM000685.1:g.44400100A>G | GRCh37 |
| NC_000023.9:g.44285044A>G | NCBI36 |
| NG_021288.1:g.7122T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378045.5:c.185+1091T>C MANE Select | ENSP00000367284.4:n.185+1091T>C | |
| ENST00000378045.4:c.185+1091T>C | ENSP00000367284.4:n.185+1091T>C | |
| ENST00000483115.1:n.360+1091T>C | ||
| NM_173794.3:c.185+1091T>C | NP_776155.1:n.185+1091T>C | |
| NM_173794.4:c.185+1091T>C MANE Select | NP_776155.1:n.185+1091T>C |