HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31357617T>C , CM000668.2:g.31357617T>C | GRCh38 |
NC_000006.11:g.31325394T>C , CM000668.1:g.31325394T>C | GRCh37 |
NC_000006.10:g.31433373T>C | NCBI36 |
NG_023187.1:g.4596A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000474381.2:n.1335A>G | ||
ENST00000481849.6:n.1335A>G | ||
ENST00000497377.6:n.1335A>G | ||
ENST00000696559.1:c.-139A>G | ENSP00000512717.1:n.-139A>G | |
ENST00000696560.1:c.-139A>G | ENSP00000512718.1:n.-139A>G | |
ENST00000696561.1:c.-139A>G | ENSP00000512719.1:n.-139A>G | |
ENST00000696562.1:c.-135-324A>G | ENSP00000512720.1:n.-135-324A>G | |
ENST00000603274.1:n.971T>C | ||
XR_926692.1:n.161A>G |