HGVS | Genome Assembly |
---|---|
NC_000008.11:g.11491599G>T , CM000670.2:g.11491599G>T | GRCh38 |
NC_000008.10:g.11349108G>T , CM000670.1:g.11349108G>T | GRCh37 |
NC_000008.9:g.11386517G>T | NCBI36 |
NG_023543.1:g.2588G>T | |
NG_023543.2:g.2588G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696154.2:n.274+4432G>T | ||
ENST00000696154.1:c.-91+4432G>T | ENSP00000512445.1:n.-91+4432G>T | |
ENST00000645242.1:c.-91+4432G>T | ENSP00000494690.1:n.-91+4432G>T |