HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38145981T= , CM000670.2:g.38145981T= | GRCh38 |
NC_000008.10:g.38003499T= , CM000670.1:g.38003499T= | GRCh37 |
NC_000008.9:g.38122656T= | NCBI36 |
NG_011827.1:g.10102A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000276449.9:c.632A= MANE Select | ENSP00000276449.3:p.Glu211= | |
ENST00000276449.8:c.632A= | ENSP00000276449.3:p.Glu211= | |
ENST00000520114.1:n.1119A= | ||
ENST00000522050.1:c.568A= | ||
NM_000349.2:c.632A= | NP_000340.2:p.Glu211= | |
XM_006716392.1:c.632A= | XP_006716455.1:p.Glu211= | |
NM_000349.3:c.632A= MANE Select | NP_000340.2:p.Glu211= |