HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94988779G= , CM000672.2:g.94988779G= | GRCh38 |
NC_000010.10:g.96748536G= , CM000672.1:g.96748536G= | GRCh37 |
NC_000010.9:g.96738526G= | NCBI36 |
NG_008385.1:g.55122G= | |
NG_008385.2:g.55622G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.1292-68G= MANE Select | ENSP00000260682.6:n.1292-68G= | |
ENST00000643112.1:c.*301-68G= | ENSP00000496202.1:n.*301-68G= | |
ENST00000260682.6:c.1292-68G= | ENSP00000260682.6:n.1292-68G= | |
NM_000771.3:c.1292-68G= | NP_000762.2:n.1292-68G= | |
NM_000771.4:c.1292-68G= MANE Select | NP_000762.2:n.1292-68G= |