Canonical Allele Identifier: CA2112648429

Gene: HS6ST3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.96193303T= , CM000675.2:g.96193303T=	GRCh38
NC_000013.10:g.96845557T= , CM000675.1:g.96845557T=	GRCh37
NC_000013.9:g.95643558T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376705.4:c.707+101734T= MANE Select	ENSP00000365895.2:n.707+101734T=
ENST00000376705.3:c.707+101734T=	ENSP00000365895.2:n.707+101734T=
NM_153456.3:c.707+101734T=	NP_703157.2:n.707+101734T=
XM_011521073.1:c.707+101734T=	XP_011519375.1:n.707+101734T=
XM_011521074.1:c.708-49353T=	XP_011519376.1:n.708-49353T=
XM_011521076.1:c.707+101734T=	XP_011519378.1:n.707+101734T=
XM_011521076.2:c.707+101734T=	XP_011519378.1:n.707+101734T=
XM_017020543.2:c.707+101734T=	XP_016876032.1:n.707+101734T=
NM_153456.4:c.707+101734T= MANE Select	NP_703157.2:n.707+101734T=