Canonical Allele Identifier: CA51062281

Gene: CTNNA2

Linked Data

• dbSNP Id: rs1048243608
• MyVariant Identifiers: chr2:g.79632279A>G (hg19) ; chr2:g.79405153A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79405153A>G , CM000664.2:g.79405153A>G	GRCh38
NC_000002.11:g.79632279A>G , CM000664.1:g.79632279A>G	GRCh37
NC_000002.10:g.79485787A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466387.5:c.-135+31140A>G	ENSP00000418191.1:n.-135+31140A>G
NM_001399737.1:c.-135+31140A>G	NP_001386666.1:n.-135+31140A>G