Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.93238417G>T , CM000675.2:g.93238417G>T | GRCh38 |
| NC_000013.10:g.93890670G>T , CM000675.1:g.93890670G>T | GRCh37 |
| NC_000013.9:g.92688671G>T | NCBI36 |
| NG_011880.1:g.16593G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005708.5:c.160+10801G>T MANE Select | NP_005699.1:n.160+10801G>T |
| ENST00000377047.9:c.160+10801G>T MANE Select | ENSP00000366246.3:n.160+10801G>T |
| NM_005708.3:c.160+10801G>T | NP_005699.1:n.160+10801G>T |
| NM_005708.4:c.160+10801G>T | NP_005699.1:n.160+10801G>T |
| ENST00000377047.8:c.160+10801G>T | ENSP00000366246.3:n.160+10801G>T |