Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.93218715A>G , CM000676.2:g.93218715A>G | GRCh38 |
| NC_000014.8:g.93685061A>G , CM000676.1:g.93685061A>G | GRCh37 |
| NC_000014.7:g.92754814A>G | NCBI36 |
| NG_051089.1:g.16660A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000013070.11:c.790A>G MANE Select | ENSP00000013070.6:p.Ser264Gly | |
| ENST00000013070.10:c.790A>G | ENSP00000013070.6:p.Ser264Gly | |
| ENST00000416753.5:c.562A>G | ENSP00000391706.2:p.Ser188Gly | |
| ENST00000553674.1:c.*491A>G | ENSP00000450470.1:n.*491A>G | |
| ENST00000553857.5:c.378+3434A>G | ||
| ENST00000555329.1:c.35A>G | ||
| NM_175748.3:c.790A>G | NP_786924.2:p.Ser264Gly | |
| NR_038150.1:n.892A>G | ||
| NM_175748.4:c.790A>G MANE Select | NP_786924.2:p.Ser264Gly | |
| NR_038150.2:n.692A>G |