Canonical Allele Identifier: CA1143538499

Gene: B3GALNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235458753C= , CM000663.2:g.235458753C=	GRCh38
NC_000001.10:g.235622061C= , CM000663.1:g.235622061C=	GRCh37
NC_000001.9:g.233688684C=	NCBI36
NG_033219.2:g.50729G=

Transcript Alleles

HGVS	Amino-acid Change
NM_152490.5:c.875G= MANE Select	NP_689703.1:p.Arg292=
ENST00000366600.8:c.875G= MANE Select	ENSP00000355559.3:p.Arg292=
NM_152490.4:c.875G=	NP_689703.1:p.Arg292=
ENST00000366600.7:c.875G=	ENSP00000355559.3:p.Arg292=
ENST00000461994.2:n.198G=
ENST00000462374.1:n.161-3069G=
ENST00000477694.5:n.198G=
ENST00000477694.6:n.1263G=
ENST00000675193.1:c.998G=	ENSP00000502069.1:p.Arg333=
ENST00000675555.1:c.653G=	ENSP00000501896.1:p.Arg218=
ENST00000676288.1:c.998G=	ENSP00000502392.1:p.Arg333=
XM_005273071.3:c.842-3069G=	XP_005273128.1:n.842-3069G=
XM_006711749.2:c.875G=	XP_006711812.1:p.Arg292=
XM_006711749.3:c.875G=	XP_006711812.1:p.Arg292=
XM_011544096.1:c.875G=	XP_011542398.1:p.Arg292=
XM_011544097.1:c.763-3069G=	XP_011542399.1:n.763-3069G=
XM_017000394.1:c.998G=	XP_016855883.1:p.Arg333=
XM_017000395.1:c.998G=	XP_016855884.1:p.Arg333=
XR_001736987.1:n.1130-3069G=
XR_001736988.1:n.1084G=
XR_001736989.1:n.1051-3069G=
XR_001736990.1:n.1013-3069G=