Canonical Allele Identifier: CA1263910774
Gene: CTNNA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405146T= , CM000664.2:g.79405146T= GRCh38
NC_000002.11:g.79632272T= , CM000664.1:g.79632272T= GRCh37
NC_000002.10:g.79485780T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31133T= ENSP00000418191.1:n.-135+31133T=
NM_001399737.1:c.-135+31133T= NP_001386666.1:n.-135+31133T=