Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149570086C>A , CM000664.2:g.149570086C>A | GRCh38 |
| NC_000002.11:g.150426600C>A , CM000664.1:g.150426600C>A | GRCh37 |
| NC_000002.10:g.150134846C>A | NCBI36 |
| NG_009189.1:g.22731G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303319.10:c.779G>T MANE Select | ENSP00000301920.5:p.Gly260Val | |
| ENST00000303319.9:c.779G>T | ENSP00000301920.5:p.Gly260Val | |
| ENST00000422782.2:c.881G>T | ENSP00000408331.2:p.Gly294Val | |
| ENST00000428879.5:c.779G>T | ENSP00000389060.1:p.Gly260Val | |
| NM_015702.2:c.779G>T | NP_056517.1:p.Gly260Val | |
| NM_015702.3:c.779G>T MANE Select | NP_056517.1:p.Gly260Val |