Canonical Allele Identifier: CA51062277
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1002311392
gnomAD v2: 2-79632268-G-A
gnomAD v3: 2-79405142-G-A
gnomAD v4: 2-79405142-G-A
MyVariant Identifiers: chr2:g.79632268G>A (hg19) chr2:g.79405142G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405142G>A , CM000664.2:g.79405142G>A GRCh38
NC_000002.11:g.79632268G>A , CM000664.1:g.79632268G>A GRCh37
NC_000002.10:g.79485776G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000466387.5:c.-135+31129G>A ENSP00000418191.1:n.-135+31129G>A
NM_001399737.1:c.-135+31129G>A NP_001386666.1:n.-135+31129G>A
Search 100 bp 5'
Search 100 bp 3'