Canonical Allele Identifier: CA1844936061
Gene: B4GALT1 HGNC NCBI

Linked Data

dbSNP Id: rs1840035672
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33122505C>T , CM000671.2:g.33122505C>T GRCh38
NC_000009.11:g.33122503C>T , CM000671.1:g.33122503C>T GRCh37
NC_000009.10:g.33112503C>T NCBI36
NG_008919.1:g.49854G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379731.5:c.649-1899G>A MANE Select ENSP00000369055.4:n.649-1899G>A
ENST00000379731.4:c.649-1899G>A ENSP00000369055.4:n.649-1899G>A
ENST00000535206.5:c.648+12684G>A ENSP00000440341.1:n.648+12684G>A
NM_001497.3:c.649-1899G>A NP_001488.2:n.649-1899G>A
XM_005251440.3:c.649-1899G>A XP_005251497.1:n.649-1899G>A
XM_005251440.5:c.649-1899G>A XP_005251497.1:n.649-1899G>A
NM_001378495.1:c.610-1899G>A NP_001365424.1:n.610-1899G>A
NM_001378496.1:c.649-1899G>A NP_001365425.1:n.649-1899G>A
NM_001378497.1:c.648+12684G>A NP_001365426.1:n.648+12684G>A
NM_001497.4:c.649-1899G>A MANE Select NP_001488.2:n.649-1899G>A
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