Canonical Allele Identifier: CA51062278
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1032452615
gnomAD v2: 2-79632269-C-A
gnomAD v3: 2-79405143-C-A
gnomAD v4: 2-79405143-C-A
MyVariant Identifiers: chr2:g.79632269C>A (hg19) chr2:g.79405143C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405143C>A , CM000664.2:g.79405143C>A GRCh38
NC_000002.11:g.79632269C>A , CM000664.1:g.79632269C>A GRCh37
NC_000002.10:g.79485777C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31130C>A ENSP00000418191.1:n.-135+31130C>A
NM_001399737.1:c.-135+31130C>A NP_001386666.1:n.-135+31130C>A
Search 100 bp 5'
Search 100 bp 3'