Canonical Allele Identifier: CA255263221

Gene: HS6ST3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.96299179G>A , CM000675.2:g.96299179G>A	GRCh38
NC_000013.10:g.96951433G>A , CM000675.1:g.96951433G>A	GRCh37
NC_000013.9:g.95749434G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376705.4:c.707+207610G>A MANE Select	ENSP00000365895.2:n.707+207610G>A
ENST00000376705.3:c.707+207610G>A	ENSP00000365895.2:n.707+207610G>A
NM_153456.3:c.707+207610G>A	NP_703157.2:n.707+207610G>A
XM_011521073.1:c.707+207610G>A	XP_011519375.1:n.707+207610G>A
XM_011521076.1:c.708-39814G>A	XP_011519378.1:n.708-39814G>A
XM_011521076.2:c.708-39814G>A	XP_011519378.1:n.708-39814G>A
XM_017020543.2:c.708-189036G>A	XP_016876032.1:n.708-189036G>A
NM_153456.4:c.707+207610G>A MANE Select	NP_703157.2:n.707+207610G>A