Canonical Allele Identifier: CA51062280
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs931183861
gnomAD v2: 2-79632276-A-G
gnomAD v3: 2-79405150-A-G
gnomAD v4: 2-79405150-A-G
MyVariant Identifiers: chr2:g.79632276A>G (hg19) chr2:g.79405150A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405150A>G , CM000664.2:g.79405150A>G GRCh38
NC_000002.11:g.79632276A>G , CM000664.1:g.79632276A>G GRCh37
NC_000002.10:g.79485784A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31137A>G ENSP00000418191.1:n.-135+31137A>G
NM_001399737.1:c.-135+31137A>G NP_001386666.1:n.-135+31137A>G
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