Canonical Allele Identifier: CA1263910786
Gene: CTNNA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405171G= , CM000664.2:g.79405171G= GRCh38
NC_000002.11:g.79632297G= , CM000664.1:g.79632297G= GRCh37
NC_000002.10:g.79485805G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31158G= ENSP00000418191.1:n.-135+31158G=
NM_001399737.1:c.-135+31158G= NP_001386666.1:n.-135+31158G=