Canonical Allele Identifier: CA1263910821
Gene: CTNNA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405228A= , CM000664.2:g.79405228A= GRCh38
NC_000002.11:g.79632354A= , CM000664.1:g.79632354A= GRCh37
NC_000002.10:g.79485862A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466387.5:c.-135+31215A= ENSP00000418191.1:n.-135+31215A=
NM_001399737.1:c.-135+31215A= NP_001386666.1:n.-135+31215A=