Canonical Allele Identifier: CA893429238

Gene: CTNNA2

Linked Data

• dbSNP Id: rs1193717485
• MyVariant Identifiers: chr2:g.79632226A>G (hg19) ; chr2:g.79405100A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79405100A>G , CM000664.2:g.79405100A>G	GRCh38
NC_000002.11:g.79632226A>G , CM000664.1:g.79632226A>G	GRCh37
NC_000002.10:g.79485734A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466387.5:c.-135+31087A>G	ENSP00000418191.1:n.-135+31087A>G
NM_001399737.1:c.-135+31087A>G	NP_001386666.1:n.-135+31087A>G