Canonical Allele Identifier: CA755165551
Gene: ANAPC1 HGNC NCBI

Linked Data

dbSNP Id: rs1260323951
gnomAD v3: 2-111618347-C-A
gnomAD v4: 2-111618347-C-A
MyVariant Identifiers: chr2:g.112375924C>A (hg19) chr2:g.111618347C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111618347C>A , CM000664.2:g.111618347C>A GRCh38
NC_000002.11:g.112375924C>A , CM000664.1:g.112375924C>A GRCh37
NC_000002.10:g.112092395C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000643447.1:c.920-3737G>T ENSP00000494863.1:n.920-3737G>T
XR_001739641.1:n.1481G>T
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