Canonical Allele Identifier: CA137993142

Gene: SUPT3H

Linked Data

• dbSNP Id: rs79435892
• gnomAD v2: 6-44777717-A-C
• gnomAD v3: 6-44809980-A-C
• gnomAD v4: 6-44809980-A-C
• MyVariant Identifiers: chr6:g.44777717A>C (hg19) ; chr6:g.44809980A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44809980A>C , CM000668.2:g.44809980A>C	GRCh38
NC_000006.11:g.44777717A>C , CM000668.1:g.44777717A>C	GRCh37
NC_000006.10:g.44885695A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475057.5:c.*53-479T>G	ENSP00000436411.1:n.*53-479T>G
XR_926319.1:n.1091-479T>G
XR_926854.1:n.341-19608A>C
XR_926855.1:n.172-19608A>C
NR_146632.1:n.1104-479T>G
NR_146633.1:n.1166-479T>G
NR_146634.1:n.1118-479T>G
NR_146635.1:n.1163-479T>G
XR_002956310.1:n.1432-479T>G
XR_926319.3:n.1091-479T>G
XR_926854.2:n.365-19608A>C
XR_926855.2:n.246-19608A>C
NR_146632.2:n.1174-479T>G
NR_146634.2:n.1160-479T>G
NR_146635.2:n.1307-479T>G