Canonical Allele Identifier: CA51062283
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1006674652
gnomAD v2: 2-79632293-GAA-G
gnomAD v3: 2-79405167-GAA-G
gnomAD v4: 2-79405167-GAA-G
MyVariant Identifiers: chr2:g.79632294_79632295del (hg19) chr2:g.79405168_79405169del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405169_79405170del , CM000664.2:g.79405169_79405170del GRCh38
NC_000002.11:g.79632295_79632296del , CM000664.1:g.79632295_79632296del GRCh37
NC_000002.10:g.79485803_79485804del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31156_-135+31157del ENSP00000418191.1:n.-135+31156_-135+31157...
NM_001399737.1:c.-135+31156_-135+31157del NP_001386666.1:n.-135+31156_-135+31157del...
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