Canonical Allele Identifier: CA1148809668
Gene: B3GALT6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1232542C= , CM000663.2:g.1232542C= GRCh38
NC_000001.10:g.1167922C= , CM000663.1:g.1167922C= GRCh37
NC_000001.9:g.1157785C= NCBI36
NG_030007.1:g.4526G=
NG_033265.1:g.5294C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379198.5:c.264C= MANE Select ENSP00000368496.2:p.Gly88=
ENST00000379198.3:c.264C= ENSP00000368496.2:p.Gly88=
NM_080605.3:c.264C= NP_542172.2:p.Gly88=
NM_080605.4:c.264C= MANE Select NP_542172.2:p.Gly88=
Search 100 bp 5'
Search 100 bp 3'