HGVS | Genome Assembly |
---|---|
NC_000002.12:g.70831745C>G , CM000664.2:g.70831745C>G | GRCh38 |
NC_000002.11:g.71058876C>G , CM000664.1:g.71058876C>G | GRCh37 |
NC_000002.10:g.70912384C>G | NCBI36 |
NG_033914.1:g.9079G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000410009.5:c.792G>C MANE Select | ENSP00000386378.3:p.Trp264Cys | |
ENST00000410009.4:c.792G>C | ENSP00000386378.3:p.Trp264Cys | |
NM_015717.4:c.792G>C | NP_056532.4:p.Trp264Cys | |
XM_011532874.1:c.792G>C | XP_011531176.1:p.Trp264Cys | |
XM_011532875.1:c.792G>C | XP_011531177.1:p.Trp264Cys | |
XM_011532876.1:c.792G>C | XP_011531178.1:p.Trp264Cys | |
XM_011532875.2:c.792G>C | XP_011531177.1:p.Trp264Cys | |
XM_011532876.2:c.792G>C | XP_011531178.1:p.Trp264Cys | |
NM_015717.5:c.792G>C MANE Select | NP_056532.4:p.Trp264Cys |