Canonical Allele Identifier: CA2832594914

Gene: HS6ST3

Genomic Alleles

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

Transcript Alleles

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