Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124875139G>T , CM000673.2:g.124875139G>T | GRCh38 |
| NC_000011.9:g.124745035G>T , CM000673.1:g.124745035G>T | GRCh37 |
| NC_000011.8:g.124250245G>T | NCBI36 |
| NG_016214.1:g.14731G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.2102G>T MANE Select | ENSP00000380903.1:p.Gly701Val | |
| ENST00000397801.5:c.2102G>T | ENSP00000380903.1:p.Gly701Val | |
| ENST00000538940.5:c.2036G>T | ENSP00000441797.1:p.Gly679Val | |
| NM_022370.3:c.2102G>T | NP_071765.2:p.Gly701Val | |
| XM_011542953.1:c.3074G>T | XP_011541255.1:p.Gly1025Val | |
| XM_017018122.1:c.2036G>T | XP_016873611.1:p.Gly679Val | |
| NM_022370.4:c.2102G>T MANE Select | NP_071765.2:p.Gly701Val |