Canonical Allele Identifier: CA835199621
Gene: AOC1 HGNC NCBI

Linked Data

dbSNP Id: rs1299969678
MyVariant Identifiers: chr7:g.150548780A>T (hg19) chr7:g.150851692A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150851692A>T , CM000669.2:g.150851692A>T GRCh38
NC_000007.13:g.150548780A>T , CM000669.1:g.150548780A>T GRCh37
NC_000007.12:g.150179713A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467291.5:c.-92-423A>T ENSP00000418328.1:n.-92-423A>T
ENST00000493429.5:c.-92-423A>T ENSP00000418614.1:n.-92-423A>T
XM_011516008.1:c.-181-423A>T XP_011514310.1:n.-181-423A>T
XM_011516009.1:c.-92-423A>T XP_011514311.1:n.-92-423A>T
XR_928169.1:n.296-10247T>A
XR_928170.1:n.426-10247T>A
XR_928171.1:n.298-10247T>A
XM_017011944.1:c.-92-423A>T XP_016867433.1:n.-92-423A>T
XM_017011945.1:c.-92-423A>T XP_016867434.1:n.-92-423A>T
XR_928169.2:n.302-10247T>A
XR_928171.2:n.302-10247T>A
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