Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21561120A>G , CM000669.2:g.21561120A>G | GRCh38 |
| NC_000007.13:g.21600738A>G , CM000669.1:g.21600738A>G | GRCh37 |
| NC_000007.12:g.21567263A>G | NCBI36 |
| NG_012886.2:g.22906A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.932A>G MANE Select | NP_001264044.1:p.Gln311Arg |
| ENST00000409508.8:c.932A>G MANE Select | ENSP00000475939.1:p.Gln311Arg |
| NM_001277115.1:c.932A>G | NP_001264044.1:p.Gln311Arg |
| ENST00000328843.10:c.932A>G | ENSP00000330671.7:p.Gln311Arg |
| ENST00000409508.7:c.932A>G | ENSP00000475939.1:p.Gln311Arg |
| ENST00000483691.1:n.128A>G | |
| ENST00000496218.1:n.30A>G | |
| ENST00000620169.4:c.932A>G | ENSP00000481693.1:p.Gln311Arg |
| XR_001745114.1:n.2794-880T>C | |
| XR_927090.1:n.564-880T>C |