Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.43949538G>A , CM000685.2:g.43949538G>A | GRCh38 |
| NC_000023.10:g.43808784G>A , CM000685.1:g.43808784G>A | GRCh37 |
| NC_000023.9:g.43693728G>A | NCBI36 |
| NG_009832.1:g.29138C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642620.1:c.*261C>T MANE Select | ENSP00000495972.1:n.*261C>T | |
| ENST00000647044.1:c.*261C>T | ENSP00000495811.1:n.*261C>T | |
| ENST00000378062.5:c.*261C>T | ENSP00000367301.5:n.*261C>T | |
| NM_000266.3:c.*261C>T | NP_000257.1:n.*261C>T | |
| NM_000266.4:c.*261C>T MANE Select | NP_000257.1:n.*261C>T |