Canonical Allele Identifier: CA137993064

Gene: SUPT3H

Linked Data

• dbSNP Id: rs994376426
• MyVariant Identifiers: chr6:g.44777594A>G (hg19) ; chr6:g.44809857A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44809857A>G , CM000668.2:g.44809857A>G	GRCh38
NC_000006.11:g.44777594A>G , CM000668.1:g.44777594A>G	GRCh37
NC_000006.10:g.44885572A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475057.5:c.*53-356T>C	ENSP00000436411.1:n.*53-356T>C
XR_926319.1:n.1091-356T>C
XR_926854.1:n.341-19731A>G
XR_926855.1:n.172-19731A>G
NR_146632.1:n.1104-356T>C
NR_146633.1:n.1166-356T>C
NR_146634.1:n.1118-356T>C
NR_146635.1:n.1163-356T>C
XR_002956310.1:n.1432-356T>C
XR_926319.3:n.1091-356T>C
XR_926854.2:n.365-19731A>G
XR_926855.2:n.246-19731A>G
NR_146632.2:n.1174-356T>C
NR_146634.2:n.1160-356T>C
NR_146635.2:n.1307-356T>C