HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44456925A>C , CM000683.2:g.44456925A>C | GRCh38 |
NC_000021.8:g.45876808A>C , CM000683.1:g.45876808A>C | GRCh37 |
NC_000021.7:g.44701236A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291592.6:c.281A>C MANE Select | ENSP00000291592.4:p.Asp94Ala | |
ENST00000291592.5:c.281A>C | ENSP00000291592.4:p.Asp94Ala | |
NM_030891.4:c.281A>C | NP_112153.1:p.Asp94Ala | |
NM_030891.5:c.281A>C | NP_112153.1:p.Asp94Ala | |
NM_030891.6:c.281A>C MANE Select | NP_112153.1:p.Asp94Ala |