Canonical Allele Identifier: CA1108694768
Gene: AOC1 HGNC NCBI

Linked Data

dbSNP Id: rs1799963248

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150861315A>G , CM000669.2:g.150861315A>G GRCh38
NC_000007.13:g.150558403A>G , CM000669.1:g.150558403A>G GRCh37
NC_000007.12:g.150189336A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360937.9:c.*106A>G MANE Select ENSP00000354193.4:n.*106A>G
ENST00000360937.8:c.*106A>G ENSP00000354193.4:n.*106A>G
ENST00000467291.5:c.*106A>G ENSP00000418328.1:n.*106A>G
ENST00000493429.5:c.*106A>G ENSP00000418614.1:n.*106A>G
XR_928169.1:n.295+15694T>C
XR_928170.1:n.425+7301T>C
XR_928171.1:n.297+15694T>C
XR_928169.2:n.301+15694T>C
XR_928171.2:n.301+15694T>C
NM_001091.4:c.*106A>G MANE Select NP_001082.2:n.*106A>G
NM_001272072.2:c.*106A>G NP_001259001.1:n.*106A>G