Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624244T>C , CM000679.2:g.41624244T>C | GRCh38 |
| NC_000017.10:g.39780496T>C , CM000679.1:g.39780496T>C | GRCh37 |
| NC_000017.9:g.37034022T>C | NCBI36 |
| NG_008625.1:g.5387A>G | |
| NG_009090.2:g.167469A>G , LRG_401:g.167469A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.266A>G MANE Select | ENSP00000308452.8:p.Gln89Arg | |
| ENST00000311208.12:c.266A>G | ENSP00000308452.8:p.Gln89Arg | |
| ENST00000463128.5:c.-312-38A>G | ENSP00000468672.1:n.-312-38A>G | |
| ENST00000491673.1:n.332A>G | ||
| ENST00000493253.5:n.53A>G | ||
| ENST00000540235.5:c.61A>G | ENSP00000441751.2:p.Arg21Gly | |
| ENST00000577817.3:c.221A>G | ENSP00000467418.1:p.Gln74Arg | |
| NM_000422.2:c.266A>G | NP_000413.1:p.Gln89Arg | |
| NM_000422.3:c.266A>G MANE Select | NP_000413.1:p.Gln89Arg |