Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48528320T>A , CM000685.2:g.48528320T>A | GRCh38 |
| NC_000023.10:g.48386708T>A , CM000685.1:g.48386708T>A | GRCh37 |
| NC_000023.9:g.48271652T>A | NCBI36 |
| NG_007452.1:g.11545T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000495186.6:c.556T>A MANE Select | ENSP00000417052.1:p.Trp186Arg | |
| ENST00000651615.1:c.469+1035T>A | ENSP00000498524.1:n.469+1035T>A | |
| ENST00000276096.10:n.514T>A | ||
| ENST00000495186.5:c.556T>A | ENSP00000417052.1:p.Trp186Arg | |
| ENST00000498425.1:n.677T>A | ||
| NM_006579.2:c.556T>A | NP_006570.1:p.Trp186Arg | |
| NM_006579.3:c.556T>A MANE Select | NP_006570.1:p.Trp186Arg |