HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42132735C>A , CM000684.2:g.42132735C>A | GRCh38 |
NC_000022.10:g.42528742C>A , CM000684.1:g.42528742C>A | GRCh37 |
NC_000022.9:g.40858686C>A | NCBI36 |
NG_008376.3:g.2257G>T | |
NG_008376.4:g.3076G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000417586.1:n.193C>A | ||
XM_011529967.1:c.-1045-899G>T | XP_011528269.1:n.-1045-899G>T |