Canonical Allele Identifier: CA893429255
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1275592442
gnomAD v3: 2-79405121-G-T
gnomAD v4: 2-79405121-G-T
MyVariant Identifiers: chr2:g.79632247G>T (hg19) chr2:g.79405121G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.79405121G>T , CM000664.2:g.79405121G>T GRCh38
NC_000002.11:g.79632247G>T , CM000664.1:g.79632247G>T GRCh37
NC_000002.10:g.79485755G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466387.5:c.-135+31108G>T ENSP00000418191.1:n.-135+31108G>T
NM_001399737.1:c.-135+31108G>T NP_001386666.1:n.-135+31108G>T
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