HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94948869A= , CM000672.2:g.94948869A= | GRCh38 |
NC_000010.10:g.96708626A= , CM000672.1:g.96708626A= | GRCh37 |
NC_000010.9:g.96698616A= | NCBI36 |
NG_008385.1:g.15212A= | |
NG_008385.2:g.15712A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.643-239A= MANE Select | ENSP00000260682.6:n.643-239A= | |
ENST00000643112.1:c.643-239A= | ENSP00000496202.1:n.643-239A= | |
ENST00000260682.6:c.643-239A= | ENSP00000260682.6:n.643-239A= | |
ENST00000473496.1:n.414-239A= | ||
NM_000771.3:c.643-239A= | NP_000762.2:n.643-239A= | |
NM_000771.4:c.643-239A= MANE Select | NP_000762.2:n.643-239A= |