HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31357562T>A , CM000668.2:g.31357562T>A | GRCh38 |
NC_000006.11:g.31325339T>A , CM000668.1:g.31325339T>A | GRCh37 |
NC_000006.10:g.31433318T>A | NCBI36 |
NG_023187.1:g.4651A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000474381.2:n.1338+52A>T | ||
ENST00000481849.6:n.1338+52A>T | ||
ENST00000497377.6:n.1338+52A>T | ||
ENST00000696559.1:c.-136+52A>T | ENSP00000512717.1:n.-136+52A>T | |
ENST00000696560.1:c.-136+52A>T | ENSP00000512718.1:n.-136+52A>T | |
ENST00000696561.1:c.-136+52A>T | ENSP00000512719.1:n.-136+52A>T | |
ENST00000696562.1:c.-135-269A>T | ENSP00000512720.1:n.-135-269A>T | |
ENST00000603274.1:n.916T>A | ||
XR_926692.1:n.164+52A>T |