HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94941710C= , CM000672.2:g.94941710C= | GRCh38 |
NC_000010.10:g.96701467C= , CM000672.1:g.96701467C= | GRCh37 |
NC_000010.9:g.96691457C= | NCBI36 |
NG_008385.1:g.8053C= | |
NG_008385.2:g.8553C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.169-148C= MANE Select | ENSP00000260682.6:n.169-148C= | |
ENST00000643112.1:c.169-148C= | ENSP00000496202.1:n.169-148C= | |
ENST00000645207.1:n.174C= | ||
ENST00000260682.6:c.169-148C= | ENSP00000260682.6:n.169-148C= | |
ENST00000461906.1:n.194-148C= | ||
NM_000771.3:c.169-148C= | NP_000762.2:n.169-148C= | |
NM_000771.4:c.169-148C= MANE Select | NP_000762.2:n.169-148C= |