HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42132688C>A , CM000684.2:g.42132688C>A | GRCh38 |
NC_000022.10:g.42528695C>A , CM000684.1:g.42528695C>A | GRCh37 |
NC_000022.9:g.40858639C>A | NCBI36 |
NG_008376.3:g.2304G>T | |
NG_008376.4:g.3123G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000417586.1:n.146C>A | ||
XM_011529967.1:c.-1045-852G>T | XP_011528269.1:n.-1045-852G>T |