Canonical Allele Identifier: CA51062285

Gene: CTNNA2

Linked Data

• dbSNP Id: rs767733372
• MyVariant Identifiers: chr2:g.79632302A>G (hg19) ; chr2:g.79405176A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79405176A>G , CM000664.2:g.79405176A>G	GRCh38
NC_000002.11:g.79632302A>G , CM000664.1:g.79632302A>G	GRCh37
NC_000002.10:g.79485810A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000466387.5:c.-135+31163A>G	ENSP00000418191.1:n.-135+31163A>G
NM_001399737.1:c.-135+31163A>G	NP_001386666.1:n.-135+31163A>G