Canonical Allele Identifier: CA2676759162

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177608835-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177608835G>T , CM000667.2:g.177608835G>T	GRCh38
NC_000005.9:g.177035836G>T , CM000667.1:g.177035836G>T	GRCh37
NC_000005.8:g.176968442G>T	NCBI36
NG_015977.1:g.13718G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.724-75G>T MANE Select	ENSP00000029410.5:n.724-75G>T
ENST00000029410.9:c.724-75G>T	ENSP00000029410.5:n.724-75G>T
ENST00000505145.1:n.1822-75G>T
ENST00000505433.5:c.*230-75G>T	ENSP00000425591.1:n.*230-75G>T
ENST00000515353.1:n.1471G>T
NM_007255.2:c.724-75G>T	NP_009186.1:n.724-75G>T
XM_005265805.2:c.382-75G>T	XP_005265862.1:n.382-75G>T
XM_006714816.2:c.244-75G>T	XP_006714879.1:n.244-75G>T
XM_011534421.1:c.382-75G>T	XP_011532723.1:n.382-75G>T
XM_006714816.4:c.244-75G>T	XP_006714879.1:n.244-75G>T
XM_017008999.2:c.382-75G>T	XP_016864488.1:n.382-75G>T
NM_007255.3:c.724-75G>T MANE Select	NP_009186.1:n.724-75G>T