Canonical Allele Identifier: CA3586396

Gene: B4GALT7

Linked Data

• ClinVar Variation Id: 2705784
• ClinVar RCV Id: RCV003892053
• dbSNP Id: rs769074597
• ExAC: 5:177031300 G / A
• gnomAD v2: 5-177031300-G-A
• gnomAD v4: 5-177604299-G-A
• MyVariant Identifiers: chr5:g.177031300G>A (hg19) ; chr5:g.177604299G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604299G>A , CM000667.2:g.177604299G>A	GRCh38
NC_000005.9:g.177031300G>A , CM000667.1:g.177031300G>A	GRCh37
NC_000005.8:g.176963906G>A	NCBI36
NG_015977.1:g.9182G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000029410.10:c.171G>A MANE Select	ENSP00000029410.5:p.Val57=
ENST00000029410.9:c.171G>A	ENSP00000029410.5:p.Val57=
ENST00000502420.1:n.150G>A
ENST00000505433.5:c.171G>A	ENSP00000425591.1:p.Val57=
ENST00000505468.1:c.-172G>A	ENSP00000420886.1:n.-172G>A
ENST00000510761.1:c.-172G>A	ENSP00000423438.1:n.-172G>A
NM_007255.2:c.171G>A	NP_009186.1:p.Val57=
XM_005265805.2:c.-172G>A	XP_005265862.1:n.-172G>A
XM_006714816.2:c.-329G>A	XP_006714879.1:n.-329G>A
XM_011534421.1:c.-172G>A	XP_011532723.1:n.-172G>A
XM_006714816.4:c.-329G>A	XP_006714879.1:n.-329G>A
XM_017008999.2:c.-172G>A	XP_016864488.1:n.-172G>A
NM_007255.3:c.171G>A MANE Select	NP_009186.1:p.Val57=