Canonical Allele Identifier: CA825049194

Gene: SUPT3H

Linked Data

• dbSNP Id: rs1304685349
• MyVariant Identifiers: chr6:g.44777894T>G (hg19) ; chr6:g.44810157T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44810157T>G , CM000668.2:g.44810157T>G	GRCh38
NC_000006.11:g.44777894T>G , CM000668.1:g.44777894T>G	GRCh37
NC_000006.10:g.44885872T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475057.5:c.*53-656A>C	ENSP00000436411.1:n.*53-656A>C
XR_926319.1:n.1091-656A>C
XR_926854.1:n.341-19431T>G
XR_926855.1:n.172-19431T>G
NR_146632.1:n.1104-656A>C
NR_146633.1:n.1166-656A>C
NR_146634.1:n.1118-656A>C
NR_146635.1:n.1163-656A>C
XR_002956310.1:n.1432-656A>C
XR_926319.3:n.1091-656A>C
XR_926854.2:n.365-19431T>G
XR_926855.2:n.246-19431T>G
NR_146632.2:n.1174-656A>C
NR_146634.2:n.1160-656A>C
NR_146635.2:n.1307-656A>C