HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942350C= , CM000672.2:g.94942350C= | GRCh38 |
NC_000010.10:g.96702107C= , CM000672.1:g.96702107C= | GRCh37 |
NC_000010.9:g.96692097C= | NCBI36 |
NG_008385.1:g.8693C= | |
NG_008385.2:g.9193C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.481+9C= MANE Select | ENSP00000260682.6:n.481+9C= | |
ENST00000643112.1:c.481+9C= | ENSP00000496202.1:n.481+9C= | |
ENST00000645207.1:n.634+9C= | ||
ENST00000260682.6:c.481+9C= | ENSP00000260682.6:n.481+9C= | |
ENST00000461906.1:n.515C= | ||
ENST00000473496.1:n.252+9C= | ||
NM_000771.3:c.481+9C= | NP_000762.2:n.481+9C= | |
NM_000771.4:c.481+9C= MANE Select | NP_000762.2:n.481+9C= |