Canonical Allele Identifier: CA137993059

Gene: SUPT3H

Linked Data

• dbSNP Id: rs1002852032
• gnomAD v3: 6-44809798-T-TA
• gnomAD v4: 6-44809798-T-TA
• MyVariant Identifiers: chr6:g.44777535_44777536insA (hg19) ; chr6:g.44809798_44809799insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44809801dup , CM000668.2:g.44809801dup	GRCh38
NC_000006.11:g.44777538dup , CM000668.1:g.44777538dup	GRCh37
NC_000006.10:g.44885516dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475057.5:c.*53-298dup	ENSP00000436411.1:n.*53-298dup
XR_926319.1:n.1091-298dup
XR_926854.1:n.341-19787dup
XR_926855.1:n.172-19787dup
NR_146632.1:n.1104-298dup
NR_146633.1:n.1166-298dup
NR_146634.1:n.1118-298dup
NR_146635.1:n.1163-298dup
XR_002956310.1:n.1432-298dup
XR_926319.3:n.1091-298dup
XR_926854.2:n.365-19787dup
XR_926855.2:n.246-19787dup
NR_146632.2:n.1174-298dup
NR_146634.2:n.1160-298dup
NR_146635.2:n.1307-298dup