Canonical Allele Identifier: CA2676759655

Gene: B4GALT7

Linked Data

• gnomAD v4: 5-177609031-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609031T>G , CM000667.2:g.177609031T>G	GRCh38
NC_000005.9:g.177036032T>G , CM000667.1:g.177036032T>G	GRCh37
NC_000005.8:g.176968638T>G	NCBI36
NG_015977.1:g.13914T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+17T>G MANE Select	ENSP00000029410.5:n.828+17T>G
ENST00000029410.9:c.828+17T>G	ENSP00000029410.5:n.828+17T>G
ENST00000505145.1:n.1926+17T>G
ENST00000505433.5:c.*334+17T>G	ENSP00000425591.1:n.*334+17T>G
ENST00000515353.1:n.1650+17T>G
NM_007255.2:c.828+17T>G	NP_009186.1:n.828+17T>G
XM_005265805.2:c.486+17T>G	XP_005265862.1:n.486+17T>G
XM_006714816.2:c.348+17T>G	XP_006714879.1:n.348+17T>G
XM_011534421.1:c.486+17T>G	XP_011532723.1:n.486+17T>G
XM_006714816.4:c.348+17T>G	XP_006714879.1:n.348+17T>G
XM_017008999.2:c.486+17T>G	XP_016864488.1:n.486+17T>G
NM_007255.3:c.828+17T>G MANE Select	NP_009186.1:n.828+17T>G