Canonical Allele Identifier: CA15220509
Gene: B3GALT1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13408808

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167709183A>G , CM000664.2:g.167709183A>G GRCh38
NC_000002.10:g.168273939A>G NCBI36
NC_000002.11:g.168565693A>G , CM000664.1:g.168565693A>G GRCh37
NG_050644.1:g.421123A>G

Transcript Alleles

HGVS Amino-acid change
XM_005246931.2:c.-352+62217A>G XP_005246988.1:p.=
XM_011512084.1:c.-352+62217A>G XP_011510386.1:p.=
XM_011512085.1:c.-368+62217A>G XP_011510387.1:p.=
XM_005246931.3:c.-352+62217A>G
XM_011512085.2:c.-368+62217A>G