HGVS | Genome Assembly |
---|---|
NC_000006.12:g.149285665G= , CM000668.2:g.149285665G= | GRCh38 |
NC_000006.11:g.149606801G= , CM000668.1:g.149606801G= | GRCh37 |
NC_000006.10:g.149648494G= | NCBI36 |
NG_021386.2:g.72742G= |
HGVS | Amino-acid Change |
---|---|
NM_001292035.2:c.6+66889G= | NP_001278964.1:n.6+66889G= |
NM_001292035.3:c.6+66889G= | NP_001278964.1:n.6+66889G= |
ENST00000606202.1:c.-121+66889G= | ENSP00000476139.1:n.-121+66889G= |