Canonical Allele Identifier: CA59890056
Gene: B3GALT1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10497324

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167302841A>G , CM000664.2:g.167302841A>G GRCh38
NC_000002.10:g.167867597A>G NCBI36
NC_000002.11:g.168159351A>G , CM000664.1:g.168159351A>G GRCh37

Transcript Alleles

HGVS Amino-acid change
XM_005246931.2:c.-511+9507A>G XP_005246988.1:p.=
XM_011512085.1:c.-527+9507A>G XP_011510387.1:p.=