HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5225604A>C , CM000673.2:g.5225604A>C | GRCh38 |
NC_000011.9:g.5246834A>C , CM000673.1:g.5246834A>C | GRCh37 |
NC_000011.8:g.5203410A>C | NCBI36 |
NG_000007.3:g.72012T>G | |
NG_059281.1:g.6468T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.438T>G | ENSP00000494175.1:p.Tyr146Ter | |
ENST00000335295.4:c.438T>G MANE Select | ENSP00000333994.3:p.Tyr146Ter | |
ENST00000633227.1:c.*254T>G | ENSP00000488004.1:n.*254T>G | |
NM_000518.4:c.438T>G | NP_000509.1:p.Tyr146Ter | |
NM_000518.5:c.438T>G MANE Select | NP_000509.1:p.Tyr146Ter |