Canonical Allele Identifier: CA12676717
Gene: AOC1 HGNC NCBI

Linked Data

dbSNP Id: rs17173637

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150832361T>C , CM000669.2:g.150832361T>C GRCh38
NC_000007.13:g.150529449T>C , CM000669.1:g.150529449T>C GRCh37
NC_000007.12:g.150160382T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000467291.5:c.-93+4959T>C ENSP00000418328.1:p.=
ENST00000493429.5:c.-93+4959T>C ENSP00000418614.1:p.=
XM_011516008.1:c.-182+4959T>C XP_011514310.1:p.=
XR_928169.1:n.352-3453A>G
XR_928170.1:n.482-3453A>G
XR_928171.1:n.354-3453A>G
XM_017011944.1:c.-93+4959T>C XP_016867433.1:p.=
XM_017011945.1:c.-93+4959T>C XP_016867434.1:p.=
XR_928169.2:n.358-3453A>G
XR_928171.2:n.358-3453A>G