Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.44540952C>A , CM000685.2:g.44540952C>A | GRCh38 |
| NC_000023.10:g.44400198C>A , CM000685.1:g.44400198C>A | GRCh37 |
| NC_000023.9:g.44285142C>A | NCBI36 |
| NG_021288.1:g.7024G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378045.5:c.185+993G>T MANE Select | ENSP00000367284.4:n.185+993G>T | |
| ENST00000378045.4:c.185+993G>T | ENSP00000367284.4:n.185+993G>T | |
| ENST00000483115.1:n.360+993G>T | ||
| NM_173794.3:c.185+993G>T | NP_776155.1:n.185+993G>T | |
| NM_173794.4:c.185+993G>T MANE Select | NP_776155.1:n.185+993G>T |