HGVS | Genome Assembly |
---|---|
NC_000015.10:g.97960941A>C , CM000677.2:g.97960941A>C | GRCh38 |
NC_000015.9:g.98504171A>C , CM000677.1:g.98504171A>C | GRCh37 |
NC_000015.8:g.96305175A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000268042.7:c.80A>C MANE Select | ENSP00000268042.6:p.Glu27Ala | |
ENST00000268042.6:c.80A>C | ENSP00000268042.6:p.Glu27Ala | |
NM_183376.2:c.80A>C | NP_899232.2:p.Glu27Ala | |
NM_183376.3:c.80A>C MANE Select | NP_899232.2:p.Glu27Ala |