Canonical Allele Identifier: CA1263910768
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1678327685

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405129C>T , CM000664.2:g.79405129C>T GRCh38
NC_000002.11:g.79632255C>T , CM000664.1:g.79632255C>T GRCh37
NC_000002.10:g.79485763C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31116C>T ENSP00000418191.1:n.-135+31116C>T
NM_001399737.1:c.-135+31116C>T NP_001386666.1:n.-135+31116C>T