Canonical Allele Identifier: CA1143808174

Gene: B3GALNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235489261C= , CM000663.2:g.235489261C=	GRCh38
NC_000001.10:g.235652566C= , CM000663.1:g.235652566C=	GRCh37
NC_000001.9:g.233719189C=	NCBI36
NG_033219.2:g.20221G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366600.8:c.268G= MANE Select	ENSP00000355559.3:p.Val90=
ENST00000675193.1:c.391G=	ENSP00000502069.1:p.Val131=
ENST00000675555.1:c.46G=	ENSP00000501896.1:p.Val16=
ENST00000676288.1:c.391G=	ENSP00000502392.1:p.Val131=
ENST00000313984.3:c.391G=	ENSP00000315678.3:p.Val131=
ENST00000366600.7:c.268G=	ENSP00000355559.3:p.Val90=
ENST00000494378.1:n.434-4746G=
ENST00000612859.4:c.261-4746G=	ENSP00000481548.1:n.261-4746G=
NM_001277155.2:c.391G=	NP_001264084.1:p.Val131=
NM_152490.4:c.268G=	NP_689703.1:p.Val90=
XM_005273071.3:c.268G=	XP_005273128.1:p.Val90=
XM_006711749.2:c.268G=	XP_006711812.1:p.Val90=
XM_011544096.1:c.268G=	XP_011542398.1:p.Val90=
XM_011544097.1:c.268G=	XP_011542399.1:p.Val90=
XM_006711749.3:c.268G=	XP_006711812.1:p.Val90=
XM_017000394.1:c.391G=	XP_016855883.1:p.Val131=
XM_017000395.1:c.391G=	XP_016855884.1:p.Val131=
XR_001736987.1:n.556G=
XR_001736988.1:n.556G=
XR_001736989.1:n.556G=
XR_001736990.1:n.439G=
NM_152490.5:c.268G= MANE Select	NP_689703.1:p.Val90=
NM_001277155.3:c.391G=	NP_001264084.1:p.Val131=