Canonical Allele Identifier: CA1603730168

Gene: B4GALT7

Linked Data

• dbSNP Id: rs1767908089
• gnomAD v4: 5-177604056-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604056T>C , CM000667.2:g.177604056T>C	GRCh38
NC_000005.9:g.177031057T>C , CM000667.1:g.177031057T>C	GRCh37
NC_000005.8:g.176963663T>C	NCBI36
NG_015977.1:g.8939T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.51-123T>C MANE Select	ENSP00000029410.5:n.51-123T>C
ENST00000029410.9:c.51-123T>C	ENSP00000029410.5:n.51-123T>C
ENST00000502420.1:n.130-223T>C
ENST00000505433.5:c.51-123T>C	ENSP00000425591.1:n.51-123T>C
ENST00000505468.1:c.-405-10T>C	ENSP00000420886.1:n.-405-10T>C
ENST00000510761.1:c.-292-123T>C	ENSP00000423438.1:n.-292-123T>C
NM_007255.2:c.51-123T>C	NP_009186.1:n.51-123T>C
XM_005265805.2:c.-292-123T>C	XP_005265862.1:n.-292-123T>C
XM_006714816.2:c.-449-123T>C	XP_006714879.1:n.-449-123T>C
XM_011534421.1:c.-292-123T>C	XP_011532723.1:n.-292-123T>C
XM_006714816.4:c.-449-123T>C	XP_006714879.1:n.-449-123T>C
XM_017008999.2:c.-292-123T>C	XP_016864488.1:n.-292-123T>C
NM_007255.3:c.51-123T>C MANE Select	NP_009186.1:n.51-123T>C