Canonical Allele Identifier: CA893429268
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1292980586

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405160T>C , CM000664.2:g.79405160T>C GRCh38
NC_000002.11:g.79632286T>C , CM000664.1:g.79632286T>C GRCh37
NC_000002.10:g.79485794T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31147T>C ENSP00000418191.1:n.-135+31147T>C
NM_001399737.1:c.-135+31147T>C NP_001386666.1:n.-135+31147T>C