Canonical Allele Identifier: CA169062982
Gene: AOC1 HGNC NCBI

Linked Data

dbSNP Id: rs34893569
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150832445dup , CM000669.2:g.150832445dup GRCh38
NC_000007.13:g.150529533dup , CM000669.1:g.150529533dup GRCh37
NC_000007.12:g.150160466dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000467291.5:c.-93+5043dup ENSP00000418328.1:n.-93+5043dup
ENST00000493429.5:c.-93+5043dup ENSP00000418614.1:n.-93+5043dup
XM_011516008.1:c.-182+5043dup XP_011514310.1:n.-182+5043dup
XR_928169.1:n.352-3536dup
XR_928170.1:n.482-3536dup
XR_928171.1:n.354-3536dup
XM_017011944.1:c.-93+5043dup XP_016867433.1:n.-93+5043dup
XM_017011945.1:c.-93+5043dup XP_016867434.1:n.-93+5043dup
XR_928169.2:n.358-3536dup
XR_928171.2:n.358-3536dup
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