Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.53051646A>C , CM000675.2:g.53051646A>C | GRCh38 |
| NC_000013.10:g.53625781A>C , CM000675.1:g.53625781A>C | GRCh37 |
| NC_000013.9:g.52523782A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006418.5:c.*875A>C MANE Select | NP_006409.3:n.*875A>C |
| ENST00000219022.3:c.*875A>C MANE Select | ENSP00000219022.2:n.*875A>C |
| NM_006418.4:c.*875A>C | NP_006409.3:n.*875A>C |
| ENST00000219022.2:c.*875A>C | ENSP00000219022.2:n.*875A>C |