Canonical Allele Identifier: CA1032633107
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1678328135
gnomAD v3: 2-79405172-ACTCAGCTGCAGAGACTCCCTCTTTCCTCCTGGCTCTGAAGT-A
gnomAD v4: 2-79405172-ACTCAGCTGCAGAGACTCCCTCTTTCCTCCTGGCTCTGAAGT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405173_79405213del , CM000664.2:g.79405173_79405213del GRCh38
NC_000002.11:g.79632299_79632339del , CM000664.1:g.79632299_79632339del GRCh37
NC_000002.10:g.79485807_79485847del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31160_-135+31200del ENSP00000418191.1:n.-135+31160_-135+31200...
NM_001399737.1:c.-135+31160_-135+31200del NP_001386666.1:n.-135+31160_-135+31200del...
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