Canonical Allele Identifier: CA51062288

Gene: CTNNA2

Linked Data

• dbSNP Id: rs988099130
• gnomAD v2: 2-79632317-C-G
• gnomAD v3: 2-79405191-C-G
• gnomAD v4: 2-79405191-C-G
• MyVariant Identifiers: chr2:g.79632317C>G (hg19) ; chr2:g.79405191C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79405191C>G , CM000664.2:g.79405191C>G	GRCh38
NC_000002.11:g.79632317C>G , CM000664.1:g.79632317C>G	GRCh37
NC_000002.10:g.79485825C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466387.5:c.-135+31178C>G	ENSP00000418191.1:n.-135+31178C>G
NM_001399737.1:c.-135+31178C>G	NP_001386666.1:n.-135+31178C>G