Canonical Allele Identifier: CA1141376316

Gene: B3GALNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235489253G= , CM000663.2:g.235489253G=	GRCh38
NC_000001.10:g.235652558G= , CM000663.1:g.235652558G=	GRCh37
NC_000001.9:g.233719181G=	NCBI36
NG_033219.2:g.20229C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366600.8:c.276C= MANE Select	ENSP00000355559.3:p.Phe92=
ENST00000675193.1:c.399C=	ENSP00000502069.1:p.Phe133=
ENST00000675555.1:c.54C=	ENSP00000501896.1:p.Phe18=
ENST00000676288.1:c.399C=	ENSP00000502392.1:p.Phe133=
ENST00000313984.3:c.399C=	ENSP00000315678.3:p.Phe133=
ENST00000366600.7:c.276C=	ENSP00000355559.3:p.Phe92=
ENST00000494378.1:n.434-4738C=
ENST00000612859.4:c.261-4738C=	ENSP00000481548.1:n.261-4738C=
NM_001277155.2:c.399C=	NP_001264084.1:p.Phe133=
NM_152490.4:c.276C=	NP_689703.1:p.Phe92=
XM_005273071.3:c.276C=	XP_005273128.1:p.Phe92=
XM_006711749.2:c.276C=	XP_006711812.1:p.Phe92=
XM_011544096.1:c.276C=	XP_011542398.1:p.Phe92=
XM_011544097.1:c.276C=	XP_011542399.1:p.Phe92=
XM_006711749.3:c.276C=	XP_006711812.1:p.Phe92=
XM_017000394.1:c.399C=	XP_016855883.1:p.Phe133=
XM_017000395.1:c.399C=	XP_016855884.1:p.Phe133=
XR_001736987.1:n.564C=
XR_001736988.1:n.564C=
XR_001736989.1:n.564C=
XR_001736990.1:n.447C=
NM_152490.5:c.276C= MANE Select	NP_689703.1:p.Phe92=
NM_001277155.3:c.399C=	NP_001264084.1:p.Phe133=