HGVS | Genome Assembly |
---|---|
NC_000008.11:g.37966292C= , CM000670.2:g.37966292C= | GRCh38 |
NC_000008.10:g.37823810C= , CM000670.1:g.37823810C= | GRCh37 |
NC_000008.9:g.37942967C= | NCBI36 |
NG_011936.1:g.5375G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000345060.5:c.178G= MANE Select | ENSP00000343782.3:p.Val60= | |
ENST00000520341.2:n.306G= | ||
ENST00000345060.4:c.178G= | ENSP00000343782.3:p.Val60= | |
ENST00000614635.1:c.178G= | ENSP00000480325.1:p.Val60= | |
NM_000025.2:c.178G= | NP_000016.1:p.Val60= | |
NM_000025.3:c.178G= MANE Select | NP_000016.1:p.Val60= |