Canonical Allele Identifier: CA13992467
Gene: LGALS3 HGNC NCBI

Linked Data

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
ENST00000254301.14:c.-4-1086T>G MANE Select ENSP00000254301.9:n.-4-1086T>G
ENST00000254301.13:c.-4-1086T>G ENSP00000254301.9:n.-4-1086T>G
ENST00000553493.5:c.-4-1086T>G ENSP00000451526.1:n.-4-1086T>G
ENST00000553755.5:n.46-1761T>G
ENST00000554715.1:c.-4-1086T>G ENSP00000451381.1:n.-4-1086T>G
NM_001177388.1:c.-4-1086T>G NP_001170859.1:n.-4-1086T>G
NM_002306.3:c.-4-1086T>G NP_002297.2:n.-4-1086T>G
XM_011536759.1:c.-4-1086T>G XP_011535061.1:n.-4-1086T>G
NM_001357678.1:c.39-1086T>G NP_001344607.1:n.39-1086T>G
NM_002306.4:c.-4-1086T>G MANE Select NP_002297.2:n.-4-1086T>G
NM_001357678.2:c.39-1086T>G NP_001344607.1:n.39-1086T>G