Canonical Allele Identifier: CA51062282

Gene: CTNNA2

Linked Data

• dbSNP Id: rs889590037
• MyVariant Identifiers: chr2:g.79632292T>A (hg19) ; chr2:g.79405166T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79405166T>A , CM000664.2:g.79405166T>A	GRCh38
NC_000002.11:g.79632292T>A , CM000664.1:g.79632292T>A	GRCh37
NC_000002.10:g.79485800T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000466387.5:c.-135+31153T>A	ENSP00000418191.1:n.-135+31153T>A
NM_001399737.1:c.-135+31153T>A	NP_001386666.1:n.-135+31153T>A