Canonical Allele Identifier: CA51062293

Gene: CTNNA2

Linked Data

• dbSNP Id: rs760733334
• gnomAD v2: 2-79632351-T-C
• gnomAD v3: 2-79405225-T-C
• gnomAD v4: 2-79405225-T-C
• MyVariant Identifiers: chr2:g.79632351T>C (hg19) ; chr2:g.79405225T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79405225T>C , CM000664.2:g.79405225T>C	GRCh38
NC_000002.11:g.79632351T>C , CM000664.1:g.79632351T>C	GRCh37
NC_000002.10:g.79485859T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466387.5:c.-135+31212T>C	ENSP00000418191.1:n.-135+31212T>C
NM_001399737.1:c.-135+31212T>C	NP_001386666.1:n.-135+31212T>C