Canonical Allele Identifier: CA137993116

Gene: SUPT3H

Linked Data

• dbSNP Id: rs557549073
• MyVariant Identifiers: chr6:g.44777699G>T (hg19) ; chr6:g.44809962G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44809962G>T , CM000668.2:g.44809962G>T	GRCh38
NC_000006.11:g.44777699G>T , CM000668.1:g.44777699G>T	GRCh37
NC_000006.10:g.44885677G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475057.5:c.*53-461C>A	ENSP00000436411.1:n.*53-461C>A
XR_926319.1:n.1091-461C>A
XR_926854.1:n.341-19626G>T
XR_926855.1:n.172-19626G>T
NR_146632.1:n.1104-461C>A
NR_146633.1:n.1166-461C>A
NR_146634.1:n.1118-461C>A
NR_146635.1:n.1163-461C>A
XR_002956310.1:n.1432-461C>A
XR_926319.3:n.1091-461C>A
XR_926854.2:n.365-19626G>T
XR_926855.2:n.246-19626G>T
NR_146632.2:n.1174-461C>A
NR_146634.2:n.1160-461C>A
NR_146635.2:n.1307-461C>A