Canonical Allele Identifier: CA13820396

Gene: HS6ST3

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.96365294G>A , CM000675.2:g.96365294G>A	GRCh38
NC_000013.10:g.97017548G>A , CM000675.1:g.97017548G>A	GRCh37
NC_000013.9:g.95815549G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376705.4:c.707+273725G>A MANE Select	ENSP00000365895.2:n.707+273725G>A
ENST00000376705.3:c.707+273725G>A	ENSP00000365895.2:n.707+273725G>A
NM_153456.3:c.707+273725G>A	NP_703157.2:n.707+273725G>A
XM_011521073.1:c.708-267781G>A	XP_011519375.1:n.708-267781G>A
XM_017020543.2:c.708-122921G>A	XP_016876032.1:n.708-122921G>A
NM_153456.4:c.707+273725G>A MANE Select	NP_703157.2:n.707+273725G>A