HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942217A= , CM000672.2:g.94942217A= | GRCh38 |
NC_000010.10:g.96701974A= , CM000672.1:g.96701974A= | GRCh37 |
NC_000010.9:g.96691964A= | NCBI36 |
NG_008385.1:g.8560A= | |
NG_008385.2:g.9060A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.357A= MANE Select | ENSP00000260682.6:p.Lys119= | |
ENST00000643112.1:c.357A= | ENSP00000496202.1:p.Lys119= | |
ENST00000645207.1:n.510A= | ||
ENST00000260682.6:c.357A= | ENSP00000260682.6:p.Lys119= | |
ENST00000461906.1:n.382A= | ||
ENST00000473496.1:n.128A= | ||
NM_000771.3:c.357A= | NP_000762.2:p.Lys119= | |
NM_000771.4:c.357A= MANE Select | NP_000762.2:p.Lys119= |