Canonical Allele Identifier: CA1752386199
Gene: AOC1 HGNC NCBI

Linked Data

dbSNP Id: rs1005389

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150846560C>A , CM000669.2:g.150846560C>A GRCh38
NC_000007.13:g.150543648C>A , CM000669.1:g.150543648C>A GRCh37
NC_000007.12:g.150174581C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000467291.5:c.-92-5555C>A ENSP00000418328.1:n.-92-5555C>A
ENST00000493429.5:c.-92-5555C>A ENSP00000418614.1:n.-92-5555C>A
XM_011516008.1:c.-181-5555C>A XP_011514310.1:n.-181-5555C>A
XM_011516009.1:c.-92-5555C>A XP_011514311.1:n.-92-5555C>A
XR_928169.1:n.296-5115G>T
XR_928170.1:n.426-5115G>T
XR_928171.1:n.298-5115G>T
XM_017011944.1:c.-92-5555C>A XP_016867433.1:n.-92-5555C>A
XM_017011945.1:c.-92-5555C>A XP_016867434.1:n.-92-5555C>A
XR_928169.2:n.302-5115G>T
XR_928171.2:n.302-5115G>T