Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.183201839T>C , CM000663.2:g.183201839T>C | GRCh38 |
| NC_000001.10:g.183170974T>C , CM000663.1:g.183170974T>C | GRCh37 |
| NC_000001.9:g.181437597T>C | NCBI36 |
| NG_007079.2:g.20576T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264144.5:c.80-6042T>C MANE Select | ENSP00000264144.4:n.80-6042T>C | |
| ENST00000264144.4:c.80-6042T>C | ENSP00000264144.4:n.80-6042T>C | |
| ENST00000493293.5:c.80-6042T>C | ENSP00000432063.1:n.80-6042T>C | |
| NM_005562.2:c.80-6042T>C | NP_005553.2:n.80-6042T>C | |
| NM_018891.2:c.80-6042T>C | NP_061486.2:n.80-6042T>C | |
| XM_017001273.2:c.80-6042T>C | XP_016856762.1:n.80-6042T>C | |
| NM_005562.3:c.80-6042T>C MANE Select | NP_005553.2:n.80-6042T>C | |
| NM_018891.3:c.80-6042T>C | NP_061486.2:n.80-6042T>C |