Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.93243089C>T , CM000675.2:g.93243089C>T | GRCh38 |
| NC_000013.10:g.93895342C>T , CM000675.1:g.93895342C>T | GRCh37 |
| NC_000013.9:g.92693343C>T | NCBI36 |
| NG_011880.1:g.21265C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005708.5:c.160+15473C>T MANE Select | NP_005699.1:n.160+15473C>T |
| ENST00000377047.9:c.160+15473C>T MANE Select | ENSP00000366246.3:n.160+15473C>T |
| NM_005708.3:c.160+15473C>T | NP_005699.1:n.160+15473C>T |
| NM_005708.4:c.160+15473C>T | NP_005699.1:n.160+15473C>T |
| ENST00000377047.8:c.160+15473C>T | ENSP00000366246.3:n.160+15473C>T |