Canonical Allele Identifier: CA1603685728

Gene: B4GALT7

Linked Data

• dbSNP Id: rs1768100937
• gnomAD v4: 5-177609029-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177609029C>G , CM000667.2:g.177609029C>G	GRCh38
NC_000005.9:g.177036030C>G , CM000667.1:g.177036030C>G	GRCh37
NC_000005.8:g.176968636C>G	NCBI36
NG_015977.1:g.13912C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.828+15C>G MANE Select	ENSP00000029410.5:n.828+15C>G
ENST00000029410.9:c.828+15C>G	ENSP00000029410.5:n.828+15C>G
ENST00000505145.1:n.1926+15C>G
ENST00000505433.5:c.*334+15C>G	ENSP00000425591.1:n.*334+15C>G
ENST00000515353.1:n.1650+15C>G
NM_007255.2:c.828+15C>G	NP_009186.1:n.828+15C>G
XM_005265805.2:c.486+15C>G	XP_005265862.1:n.486+15C>G
XM_006714816.2:c.348+15C>G	XP_006714879.1:n.348+15C>G
XM_011534421.1:c.486+15C>G	XP_011532723.1:n.486+15C>G
XM_006714816.4:c.348+15C>G	XP_006714879.1:n.348+15C>G
XM_017008999.2:c.486+15C>G	XP_016864488.1:n.486+15C>G
NM_007255.3:c.828+15C>G MANE Select	NP_009186.1:n.828+15C>G