Canonical Allele Identifier: CA169071210

Gene: AOC1

Linked Data

• dbSNP Id: rs960733964
• MyVariant Identifiers: chr7:g.150543673A>T (hg19) ; chr7:g.150846585A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150846585A>T , CM000669.2:g.150846585A>T	GRCh38
NC_000007.13:g.150543673A>T , CM000669.1:g.150543673A>T	GRCh37
NC_000007.12:g.150174606A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000467291.5:c.-92-5530A>T	ENSP00000418328.1:n.-92-5530A>T
ENST00000493429.5:c.-92-5530A>T	ENSP00000418614.1:n.-92-5530A>T
XM_011516008.1:c.-181-5530A>T	XP_011514310.1:n.-181-5530A>T
XM_011516009.1:c.-92-5530A>T	XP_011514311.1:n.-92-5530A>T
XR_928169.1:n.296-5140T>A
XR_928170.1:n.426-5140T>A
XR_928171.1:n.298-5140T>A
XM_017011944.1:c.-92-5530A>T	XP_016867433.1:n.-92-5530A>T
XM_017011945.1:c.-92-5530A>T	XP_016867434.1:n.-92-5530A>T
XR_928169.2:n.302-5140T>A
XR_928171.2:n.302-5140T>A