Canonical Allele Identifier: CA893429295

Gene: CTNNA2

Linked Data

• dbSNP Id: rs1341964545
• gnomAD v3: 2-79405216-C-T
• gnomAD v4: 2-79405216-C-T
• MyVariant Identifiers: chr2:g.79632342C>T (hg19) ; chr2:g.79405216C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79405216C>T , CM000664.2:g.79405216C>T	GRCh38
NC_000002.11:g.79632342C>T , CM000664.1:g.79632342C>T	GRCh37
NC_000002.10:g.79485850C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466387.5:c.-135+31203C>T	ENSP00000418191.1:n.-135+31203C>T
NM_001399737.1:c.-135+31203C>T	NP_001386666.1:n.-135+31203C>T