Canonical Allele Identifier: CA349250015

Gene: B3GALT1 B3GALT1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167869626C>T , CM000664.2:g.167869626C>T	GRCh38
NC_000002.11:g.168726136C>T , CM000664.1:g.168726136C>T	GRCh37
NC_000002.10:g.168434382C>T	NCBI36
NG_050644.1:g.581566C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392690.4:c.587C>T (B3GALT1) MANE Select	ENSP00000376456.2:p.Thr196Ile
ENST00000392690.3:c.587C>T (B3GALT1)	ENSP00000376456.2:p.Thr196Ile
NM_020981.3:c.587C>T (B3GALT1)	NP_066191.1:p.Thr196Ile
NR_131227.1:n.328+114G>A (B3GALT1-AS1)
XM_005246931.2:c.587C>T (B3GALT1)	XP_005246988.1:p.Thr196Ile
XM_006712819.2:c.587C>T (B3GALT1)	XP_006712882.1:p.Thr196Ile
XM_011512084.1:c.587C>T (B3GALT1)	XP_011510386.1:p.Thr196Ile
XM_011512085.1:c.587C>T (B3GALT1)	XP_011510387.1:p.Thr196Ile
XM_005246931.3:c.587C>T (B3GALT1)	XP_005246988.1:p.Thr196Ile
XM_006712819.3:c.587C>T (B3GALT1)	XP_006712882.1:p.Thr196Ile
XM_011512085.2:c.587C>T (B3GALT1)	XP_011510387.1:p.Thr196Ile
NM_020981.4:c.587C>T (B3GALT1) MANE Select	NP_066191.1:p.Thr196Ile