HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44456843G= , CM000683.2:g.44456843G= | GRCh38 |
NC_000021.8:g.45876726G= , CM000683.1:g.45876726G= | GRCh37 |
NC_000021.7:g.44701154G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291592.6:c.199G= MANE Select | ENSP00000291592.4:p.Val67= | |
ENST00000291592.5:c.199G= | ENSP00000291592.4:p.Val67= | |
NM_030891.4:c.199G= | NP_112153.1:p.Val67= | |
NM_030891.5:c.199G= | NP_112153.1:p.Val67= | |
NM_030891.6:c.199G= MANE Select | NP_112153.1:p.Val67= |