Canonical Allele Identifier: CA13992467
Gene: LGALS3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1009977

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.55136284T>G , CM000676.2:g.55136284T>G GRCh38
NC_000014.8:g.55603002T>G , CM000676.1:g.55603002T>G GRCh37
NC_000014.7:g.54672755T>G NCBI36
NG_017089.1:g.12068T>G

Transcript Alleles

HGVS Amino-acid change
NM_001177388.1:c.-4-1086T>G VV NP_001170859.1:p.=
NM_002306.3:c.-4-1086T>G VV NP_002297.2:p.=
XM_011536759.1:c.-4-1086T>G XP_011535061.1:p.=
NM_001357678.1:c.39-1086T>G VV NP_001344607.1:p.=
NM_002306.4:c.-4-1086T>G VV MANE Preferred NP_002297.2:p.=
ENST00000254301.13:c.-4-1086T>G ENSP00000254301.9:p.=
ENST00000553493.5:c.-4-1086T>G ENSP00000451526.1:p.=
ENST00000553755.5:n.46-1761T>G
ENST00000554715.1:c.-4-1086T>G ENSP00000451381.1:p.=