Canonical Allele Identifier: CA535369419
Gene: ANAPC1 HGNC NCBI

Linked Data

dbSNP Id: rs1232577612
gnomAD v2: 2-112376009-T-C
gnomAD v3: 2-111618432-T-C
gnomAD v4: 2-111618432-T-C
MyVariant Identifiers: chr2:g.112376009T>C (hg19) chr2:g.111618432T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111618432T>C , CM000664.2:g.111618432T>C GRCh38
NC_000002.11:g.112376009T>C , CM000664.1:g.112376009T>C GRCh37
NC_000002.10:g.112092480T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000643447.1:c.920-3822A>G ENSP00000494863.1:n.920-3822A>G
XR_001739641.1:n.1396A>G
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