Canonical Allele Identifier: CA023895
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82732
ClinVar RCV Id: RCV000073721
dbSNP Id: rs75612255
MyVariant Identifiers: chr5:g.112073240T>C (hg19) chr5:g.112737543T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112737543T>C , CM000667.2:g.112737543T>C GRCh38
NC_000005.9:g.112073240T>C , CM000667.1:g.112073240T>C GRCh37
NC_000005.8:g.112101139T>C NCBI36
NG_008481.4:g.50023T>C , LRG_130:g.50023T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000505350.2:c.166-17330T>C ENSP00000481752.1:n.166-17330T>C
ENST00000507379.6:c.166-28783T>C ENSP00000423224.2:n.166-28783T>C
ENST00000509732.6:c.-18-17330T>C ENSP00000426541.2:n.-18-17330T>C
ENST00000505350.1:c.166-17330T>C ENSP00000481752.1:n.166-17330T>C
ENST00000507379.5:c.166-28783T>C ENSP00000423224.1:n.166-28783T>C
ENST00000509732.5:c.-18-17330T>C ENSP00000426541.1:n.-18-17330T>C
NM_001127511.2:c.166-28783T>C NP_001120983.2:n.166-28783T>C
NM_001354895.1:c.-18-17330T>C NP_001341824.1:n.-18-17330T>C
NM_001354897.1:c.166-28783T>C NP_001341826.1:n.166-28783T>C
NM_001354902.1:c.166-28783T>C NP_001341831.1:n.166-28783T>C
NM_001127511.3:c.166-28783T>C NP_001120983.2:n.166-28783T>C
NM_001354895.2:c.-18-17330T>C NP_001341824.1:n.-18-17330T>C
NM_001354897.2:c.166-28783T>C NP_001341826.1:n.166-28783T>C
NM_001354902.2:c.166-28783T>C NP_001341831.1:n.166-28783T>C
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