Canonical Allele Identifier: CA658655894
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469825
ClinVar RCV Id: RCV003742645
dbSNP Id: rs964366695

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707594C>G , CM000667.2:g.112707594C>G GRCh38
NC_000005.9:g.112043291C>G , CM000667.1:g.112043291C>G GRCh37
NC_000005.8:g.112071190C>G NCBI36
NG_008481.4:g.20074C>G , LRG_130:g.20074C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.-124C>G ENSP00000481752.1:n.-124C>G
ENST00000507379.6:c.-124C>G ENSP00000423224.2:n.-124C>G
ENST00000509732.6:c.-74C>G ENSP00000426541.2:n.-74C>G
ENST00000505350.1:c.-124C>G ENSP00000481752.1:n.-124C>G
ENST00000507379.5:c.-124C>G ENSP00000423224.1:n.-124C>G
ENST00000509732.5:c.-74C>G ENSP00000426541.1:n.-74C>G
NM_001127511.2:c.-124C>G NP_001120983.2:n.-124C>G
NM_001354895.1:c.-307C>G NP_001341824.1:n.-307C>G
NM_001354897.1:c.-124C>G NP_001341826.1:n.-124C>G
NM_001354902.1:c.-124C>G NP_001341831.1:n.-124C>G
NM_001127511.3:c.-124C>G NP_001120983.2:n.-124C>G
NM_001354895.2:c.-307C>G NP_001341824.1:n.-307C>G
NM_001354897.2:c.-124C>G NP_001341826.1:n.-124C>G
NM_001354902.2:c.-124C>G NP_001341831.1:n.-124C>G