Canonical Allele Identifier: CA1263910827
Gene: CTNNA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405238A= , CM000664.2:g.79405238A= GRCh38
NC_000002.11:g.79632364A= , CM000664.1:g.79632364A= GRCh37
NC_000002.10:g.79485872A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466387.5:c.-135+31225A= ENSP00000418191.1:n.-135+31225A=
NM_001399737.1:c.-135+31225A= NP_001386666.1:n.-135+31225A=