Canonical Allele Identifier: CA137993144

Gene: SUPT3H

Linked Data

• dbSNP Id: rs896738227
• gnomAD v2: 6-44777720-C-G
• gnomAD v3: 6-44809983-C-G
• gnomAD v4: 6-44809983-C-G
• MyVariant Identifiers: chr6:g.44777720C>G (hg19) ; chr6:g.44809983C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44809983C>G , CM000668.2:g.44809983C>G	GRCh38
NC_000006.11:g.44777720C>G , CM000668.1:g.44777720C>G	GRCh37
NC_000006.10:g.44885698C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475057.5:c.*53-482G>C	ENSP00000436411.1:n.*53-482G>C
XR_926319.1:n.1091-482G>C
XR_926854.1:n.341-19605C>G
XR_926855.1:n.172-19605C>G
NR_146632.1:n.1104-482G>C
NR_146633.1:n.1166-482G>C
NR_146634.1:n.1118-482G>C
NR_146635.1:n.1163-482G>C
XR_002956310.1:n.1432-482G>C
XR_926319.3:n.1091-482G>C
XR_926854.2:n.365-19605C>G
XR_926855.2:n.246-19605C>G
NR_146632.2:n.1174-482G>C
NR_146634.2:n.1160-482G>C
NR_146635.2:n.1307-482G>C