Canonical Allele Identifier: CA12488496
Gene: AOC1 HGNC NCBI

Linked Data

dbSNP Id: rs1005390

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150846633T>G , CM000669.2:g.150846633T>G GRCh38
NC_000007.13:g.150543721T>G , CM000669.1:g.150543721T>G GRCh37
NC_000007.12:g.150174654T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000467291.5:c.-92-5482T>G ENSP00000418328.1:p.=
ENST00000493429.5:c.-92-5482T>G ENSP00000418614.1:p.=
XM_011516008.1:c.-181-5482T>G XP_011514310.1:p.=
XM_011516009.1:c.-92-5482T>G XP_011514311.1:p.=
XR_928169.1:n.296-5188A>C
XR_928170.1:n.426-5188A>C
XR_928171.1:n.298-5188A>C
XM_017011944.1:c.-92-5482T>G XP_016867433.1:p.=
XM_017011945.1:c.-92-5482T>G XP_016867434.1:p.=
XR_928169.2:n.302-5188A>C
XR_928171.2:n.302-5188A>C