HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44456942A>G , CM000683.2:g.44456942A>G | GRCh38 |
NC_000021.8:g.45876825A>G , CM000683.1:g.45876825A>G | GRCh37 |
NC_000021.7:g.44701253A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291592.6:c.298A>G MANE Select | ENSP00000291592.4:p.Ile100Val | |
ENST00000291592.5:c.298A>G | ENSP00000291592.4:p.Ile100Val | |
NM_030891.4:c.298A>G | NP_112153.1:p.Ile100Val | |
NM_030891.5:c.298A>G | NP_112153.1:p.Ile100Val | |
NM_030891.6:c.298A>G MANE Select | NP_112153.1:p.Ile100Val |