Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83508971G>A , CM000685.2:g.83508971G>A | GRCh38 |
| NC_000023.10:g.82763979G>A , CM000685.1:g.82763979G>A | GRCh37 |
| NC_000023.9:g.82650635G>A | NCBI36 |
| NG_009936.2:g.5711G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000644024.2:c.647G>A MANE Select | ENSP00000495996.1:p.Gly216Glu | |
| ENST00000373200.4:c.647G>A | ENSP00000362296.2:p.Gly216Glu | |
| NM_000307.4:c.647G>A | NP_000298.3:p.Gly216Glu | |
| NM_000307.5:c.647G>A MANE Select | NP_000298.3:p.Gly216Glu |