Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86578705C>T , CM000670.2:g.86578705C>T | GRCh38 |
| NC_000008.10:g.87590933C>T , CM000670.1:g.87590933C>T | GRCh37 |
| NC_000008.9:g.87660049C>T | NCBI36 |
| NG_016980.1:g.169971G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_019098.5:c.2087G>A MANE Select | NP_061971.3:p.Arg696Gln |
| ENST00000320005.6:c.2087G>A MANE Select | ENSP00000316605.5:p.Arg696Gln |
| NM_019098.4:c.2087G>A | NP_061971.3:p.Arg696Gln |
| ENST00000320005.5:c.2087G>A | ENSP00000316605.5:p.Arg696Gln |
| ENST00000517327.5:c.260G>A | ENSP00000428329.1:p.Arg87Gln |
| ENST00000681546.1:n.1907G>A | |
| ENST00000681746.1:c.*498G>A | ENSP00000505959.1:n.*498G>A |
| XM_011517138.1:c.1673G>A | XP_011515440.1:p.Arg558Gln |
| XM_011517138.2:c.1673G>A | XP_011515440.1:p.Arg558Gln |