Canonical Allele Identifier: CA566955565

Gene: SUPT3H

Linked Data

• dbSNP Id: rs1370362133
• gnomAD v2: 6-44777724-C-A
• gnomAD v3: 6-44809987-C-A
• gnomAD v4: 6-44809987-C-A
• MyVariant Identifiers: chr6:g.44777724C>A (hg19) ; chr6:g.44809987C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44809987C>A , CM000668.2:g.44809987C>A	GRCh38
NC_000006.11:g.44777724C>A , CM000668.1:g.44777724C>A	GRCh37
NC_000006.10:g.44885702C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475057.5:c.*53-486G>T	ENSP00000436411.1:n.*53-486G>T
XR_926319.1:n.1091-486G>T
XR_926854.1:n.341-19601C>A
XR_926855.1:n.172-19601C>A
NR_146632.1:n.1104-486G>T
NR_146633.1:n.1166-486G>T
NR_146634.1:n.1118-486G>T
NR_146635.1:n.1163-486G>T
XR_002956310.1:n.1432-486G>T
XR_926319.3:n.1091-486G>T
XR_926854.2:n.365-19601C>A
XR_926855.2:n.246-19601C>A
NR_146632.2:n.1174-486G>T
NR_146634.2:n.1160-486G>T
NR_146635.2:n.1307-486G>T