Canonical Allele Identifier: CA12458237
Gene: AHR HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.17247645A>T
GRCh37 chr7:g.17287269A>T
gnomAD v2:
7:17287269 A / T
gnomAD v3:
7:17247645 A / T
gnomAD v4:
chr7-17247645-A-T
Joint Max Group AF 0.62106118 (NFE)
Genomes Max Group AF 0.6210931 (NFE)
Exomes Max Group AF 0.26084543 (NFE)
dbSNP:
6968865
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247645A>T , CM000669.2:g.17247645A>T GRCh38
NC_000007.13:g.17287269A>T , CM000669.1:g.17287269A>T GRCh37
NC_000007.12:g.17253794A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-284A>T ENSP00000495987.1:n.-284A>T
XR_927073.2:n.861+11607T>A
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