Canonical Allele Identifier: CA1625150154
Gene: SUPT3H HGNC NCBI

Linked Data

dbSNP Id: rs1766390403

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44809825_44809828dup , CM000668.2:g.44809825_44809828dup GRCh38
NC_000006.11:g.44777562_44777565dup , CM000668.1:g.44777562_44777565dup GRCh37
NC_000006.10:g.44885540_44885543dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475057.5:c.*53-326_*53-323dup ENSP00000436411.1:n.*53-326_*53-323dup
XR_926319.1:n.1091-326_1091-323dup
XR_926854.1:n.341-19763_341-19760dup
XR_926855.1:n.172-19763_172-19760dup
NR_146632.1:n.1104-326_1104-323dup
NR_146633.1:n.1166-326_1166-323dup
NR_146634.1:n.1118-326_1118-323dup
NR_146635.1:n.1163-326_1163-323dup
XR_002956310.1:n.1432-326_1432-323dup
XR_926319.3:n.1091-326_1091-323dup
XR_926854.2:n.365-19763_365-19760dup
XR_926855.2:n.246-19763_246-19760dup
NR_146632.2:n.1174-326_1174-323dup
NR_146634.2:n.1160-326_1160-323dup
NR_146635.2:n.1307-326_1307-323dup