HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942295T= , CM000672.2:g.94942295T= | GRCh38 |
NC_000010.10:g.96702052T= , CM000672.1:g.96702052T= | GRCh37 |
NC_000010.9:g.96692042T= | NCBI36 |
NG_008385.1:g.8638T= | |
NG_008385.2:g.9138T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.435T= MANE Select | ENSP00000260682.6:p.Val145= | |
ENST00000643112.1:c.435T= | ENSP00000496202.1:p.Val145= | |
ENST00000645207.1:n.588T= | ||
ENST00000260682.6:c.435T= | ENSP00000260682.6:p.Val145= | |
ENST00000461906.1:n.460T= | ||
ENST00000473496.1:n.206T= | ||
NM_000771.3:c.435T= | NP_000762.2:p.Val145= | |
NM_000771.4:c.435T= MANE Select | NP_000762.2:p.Val145= |