HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31357255C>A , CM000668.2:g.31357255C>A | GRCh38 |
NC_000006.11:g.31325032C>A , CM000668.1:g.31325032C>A | GRCh37 |
NC_000006.10:g.31433011C>A | NCBI36 |
NG_023187.1:g.4958G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000474381.2:n.1377G>T | ||
ENST00000481849.6:n.1377G>T | ||
ENST00000497377.6:n.1377G>T | ||
ENST00000696559.1:c.-97G>T | ENSP00000512717.1:n.-97G>T | |
ENST00000696560.1:c.-97G>T | ENSP00000512718.1:n.-97G>T | |
ENST00000696561.1:c.-97G>T | ENSP00000512719.1:n.-97G>T | |
ENST00000696562.1:c.-97G>T | ENSP00000512720.1:n.-97G>T | |
ENST00000603274.1:n.609C>A |