Canonical Allele Identifier: CA169071230

Gene: AOC1

Linked Data

• dbSNP Id: rs973203861
• gnomAD v3: 7-150846638-C-T
• gnomAD v4: 7-150846638-C-T
• MyVariant Identifiers: chr7:g.150543726C>T (hg19) ; chr7:g.150846638C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150846638C>T , CM000669.2:g.150846638C>T	GRCh38
NC_000007.13:g.150543726C>T , CM000669.1:g.150543726C>T	GRCh37
NC_000007.12:g.150174659C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467291.5:c.-92-5477C>T	ENSP00000418328.1:n.-92-5477C>T
ENST00000493429.5:c.-92-5477C>T	ENSP00000418614.1:n.-92-5477C>T
XM_011516008.1:c.-181-5477C>T	XP_011514310.1:n.-181-5477C>T
XM_011516009.1:c.-92-5477C>T	XP_011514311.1:n.-92-5477C>T
XR_928169.1:n.296-5193G>A
XR_928170.1:n.426-5193G>A
XR_928171.1:n.298-5193G>A
XM_017011944.1:c.-92-5477C>T	XP_016867433.1:n.-92-5477C>T
XM_017011945.1:c.-92-5477C>T	XP_016867434.1:n.-92-5477C>T
XR_928169.2:n.302-5193G>A
XR_928171.2:n.302-5193G>A