HGVS | Genome Assembly |
---|---|
NC_000024.10:g.13765774T>C , CM000686.2:g.13765774T>C | GRCh38 |
NC_000024.9:g.15877654T>C , CM000686.1:g.15877654T>C | GRCh37 |
NC_000024.8:g.14387048T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000652544.1:n.684+10985T>C | ||
ENST00000430079.5:n.429+10985T>C | ||
ENST00000460561.1:n.212+10985T>C | ||
ENST00000472227.5:n.350+13769T>C |