Canonical Allele Identifier: CA10861213
Gene: LGALS8 HGNC NCBI

Linked Data

dbSNP Id: rs4659682

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236518948A>G , CM000663.2:g.236518948A>G GRCh38
NC_000001.10:g.236682248A>G , CM000663.1:g.236682248A>G GRCh37
NC_000001.9:g.234748871A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000352231.6:c.-104+448A>G ENSP00000309576.2:n.-104+448A>G
ENST00000406509.7:c.-318+448A>G ENSP00000385999.3:n.-318+448A>G
ENST00000430527.6:c.-104+448A>G ENSP00000398630.2:n.-104+448A>G
ENST00000454943.6:c.-196+448A>G ENSP00000405504.2:n.-196+448A>G
ENST00000481485.5:c.-196+664A>G ENSP00000435632.1:n.-196+664A>G
ENST00000526589.5:c.-432+448A>G ENSP00000435460.1:n.-432+448A>G
ENST00000527974.5:c.-104+664A>G ENSP00000431398.1:n.-104+664A>G
ENST00000529489.5:c.-226+448A>G ENSP00000437007.1:n.-226+448A>G
NM_201545.2:c.-104+448A>G NP_963839.1:n.-104+448A>G