Canonical Allele Identifier: CA423759090

Gene: B3GALNT2

Linked Data

• MyVariant Identifiers: chr1:g.235652528A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235489223A>G , CM000663.2:g.235489223A>G	GRCh38
NC_000001.10:g.235652528A>G , CM000663.1:g.235652528A>G	GRCh37
NC_000001.9:g.233719151A>G	NCBI36
NG_033219.2:g.20259T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366600.8:c.306T>C MANE Select	ENSP00000355559.3:p.Pro102=
ENST00000675193.1:c.429T>C	ENSP00000502069.1:p.Pro143=
ENST00000675555.1:c.84T>C	ENSP00000501896.1:p.Pro28=
ENST00000676288.1:c.429T>C	ENSP00000502392.1:p.Pro143=
ENST00000313984.3:c.429T>C	ENSP00000315678.3:p.Pro143=
ENST00000366600.7:c.306T>C	ENSP00000355559.3:p.Pro102=
ENST00000494378.1:n.434-4708T>C
ENST00000612859.4:c.261-4708T>C	ENSP00000481548.1:n.261-4708T>C
NM_001277155.2:c.429T>C	NP_001264084.1:p.Pro143=
NM_152490.4:c.306T>C	NP_689703.1:p.Pro102=
XM_005273071.3:c.306T>C	XP_005273128.1:p.Pro102=
XM_006711749.2:c.306T>C	XP_006711812.1:p.Pro102=
XM_011544096.1:c.306T>C	XP_011542398.1:p.Pro102=
XM_011544097.1:c.306T>C	XP_011542399.1:p.Pro102=
XM_006711749.3:c.306T>C	XP_006711812.1:p.Pro102=
XM_017000394.1:c.429T>C	XP_016855883.1:p.Pro143=
XM_017000395.1:c.429T>C	XP_016855884.1:p.Pro143=
XR_001736987.1:n.594T>C
XR_001736988.1:n.594T>C
XR_001736989.1:n.594T>C
XR_001736990.1:n.477T>C
NM_152490.5:c.306T>C MANE Select	NP_689703.1:p.Pro102=
NM_001277155.3:c.429T>C	NP_001264084.1:p.Pro143=