Canonical Allele Identifier: CA2699635658

Gene: CTNNA2

Linked Data

• dbSNP Id: rs2104484476

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79405078G>A , CM000664.2:g.79405078G>A	GRCh38
NC_000002.11:g.79632204G>A , CM000664.1:g.79632204G>A	GRCh37
NC_000002.10:g.79485712G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466387.5:c.-135+31065G>A	ENSP00000418191.1:n.-135+31065G>A
NM_001399737.1:c.-135+31065G>A	NP_001386666.1:n.-135+31065G>A