Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124874137G>A , CM000673.2:g.124874137G>A | GRCh38 |
| NC_000011.9:g.124744033G>A , CM000673.1:g.124744033G>A | GRCh37 |
| NC_000011.8:g.124249243G>A | NCBI36 |
| NG_016214.1:g.13729G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.1852G>A MANE Select | ENSP00000380903.1:p.Gly618Ser | |
| ENST00000397801.5:c.1852G>A | ENSP00000380903.1:p.Gly618Ser | |
| ENST00000538940.5:c.1786G>A | ENSP00000441797.1:p.Gly596Ser | |
| NM_022370.3:c.1852G>A | NP_071765.2:p.Gly618Ser | |
| XM_011542953.1:c.2824G>A | XP_011541255.1:p.Gly942Ser | |
| XM_017018122.1:c.1786G>A | XP_016873611.1:p.Gly596Ser | |
| NM_022370.4:c.1852G>A MANE Select | NP_071765.2:p.Gly618Ser |