HGVS | Genome Assembly |
---|---|
NC_000005.10:g.45461885G= , CM000667.2:g.45461885G= | GRCh38 |
NC_000005.9:g.45461987G= , CM000667.1:g.45461987G= | GRCh37 |
NC_000005.8:g.45497744G= | NCBI36 |
NG_042183.1:g.239234C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303230.6:c.972C= MANE Select | ENSP00000307342.4:p.Asp324= | |
ENST00000637305.1:n.135C= | ||
ENST00000673735.1:c.972C= | ENSP00000501107.1:p.Asp324= | |
ENST00000303230.5:c.972C= | ENSP00000307342.4:p.Asp324= | |
NM_021072.3:c.972C= | NP_066550.2:p.Asp324= | |
NM_021072.4:c.972C= MANE Select | NP_066550.2:p.Asp324= |