Canonical Allele Identifier: CA1263910770
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1678327705

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405137G>T , CM000664.2:g.79405137G>T GRCh38
NC_000002.11:g.79632263G>T , CM000664.1:g.79632263G>T GRCh37
NC_000002.10:g.79485771G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31124G>T ENSP00000418191.1:n.-135+31124G>T
NM_001399737.1:c.-135+31124G>T NP_001386666.1:n.-135+31124G>T