Canonical Allele Identifier: CA324100861
Gene: LGALS2 HGNC NCBI

Linked Data

dbSNP Id: rs909390248
gnomAD v2: 22-37972549-A-G
gnomAD v3: 22-37576542-A-G
gnomAD v4: 22-37576542-A-G
MyVariant Identifiers: chr22:g.37972549A>G (hg19) chr22:g.37576542A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37576542A>G , CM000684.2:g.37576542A>G GRCh38
NC_000022.10:g.37972549A>G , CM000684.1:g.37972549A>G GRCh37
NC_000022.9:g.36302495A>G NCBI36
NG_012096.1:g.8476T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000215886.6:c.6+3358T>C MANE Select ENSP00000215886.4:n.6+3358T>C
ENST00000215886.5:c.6+3358T>C ENSP00000215886.4:n.6+3358T>C
ENST00000416480.1:c.6+3358T>C ENSP00000407351.1:n.6+3358T>C
NM_006498.2:c.6+3358T>C NP_006489.1:n.6+3358T>C
NM_006498.3:c.6+3358T>C MANE Select NP_006489.1:n.6+3358T>C
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