HGVS | Genome Assembly |
---|---|
NC_000011.10:g.17553481G= , CM000673.2:g.17553481G= | GRCh38 |
NC_000011.9:g.17575028G= , CM000673.1:g.17575028G= | GRCh37 |
NC_000011.8:g.17531604G= | NCBI36 |
NG_033191.1:g.11109G= | |
NG_033191.2:g.11109G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000399391.7:c.538G= | ENSP00000382323.2:p.Gly180= | |
ENST00000399397.6:c.502G= MANE Select | ENSP00000382329.2:p.Gly168= | |
ENST00000399391.6:c.538G= | ENSP00000382323.2:p.Gly180= | |
ENST00000399397.5:c.502G= | ENSP00000382329.2:p.Gly168= | |
ENST00000498332.5:n.408G= | ||
NM_001277269.1:c.538G= | NP_001264198.1:p.Gly180= | |
NM_001292063.1:c.502G= | NP_001278992.1:p.Gly168= | |
NM_001277269.2:c.538G= | NP_001264198.1:p.Gly180= | |
NM_001292063.2:c.502G= MANE Select | NP_001278992.1:p.Gly168= |