Canonical Allele Identifier: CA646786501

Gene: CTNNA2

Linked Data

• dbSNP Id: rs1356444763
• COSMIC: COSN17284211
• MyVariant Identifiers: chr2:g.79632293G>A (hg19) ; chr2:g.79405167G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79405167G>A , CM000664.2:g.79405167G>A	GRCh38
NC_000002.11:g.79632293G>A , CM000664.1:g.79632293G>A	GRCh37
NC_000002.10:g.79485801G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000466387.5:c.-135+31154G>A	ENSP00000418191.1:n.-135+31154G>A
NM_001399737.1:c.-135+31154G>A	NP_001386666.1:n.-135+31154G>A