Canonical Allele Identifier: CA16293179
Gene: AHR HGNC NCBI
dbSNP:
10247158
gnomAD v2:
7:17325168 A / T
gnomAD v3:
7:17285544 A / T
gnomAD v4:
chr7-17285544-A-T
Joint Max Group AF 0.2595304 (AMR)
Genomes Max Group AF 0.2595304 (AMR)
MyVariant.info:
GRCh38 chr7:g.17285544A>T
GRCh37 chr7:g.17325168A>T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285544A>T , CM000669.2:g.17285544A>T GRCh38
NC_000007.13:g.17325168A>T , CM000669.1:g.17325168A>T GRCh37
NC_000007.12:g.17291693A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10753A>T ENSP00000495987.1:n.-202-10753A>T
XR_927069.1:n.567+699T>A
XR_927070.1:n.567+699T>A
XR_927071.1:n.567+699T>A
XR_927072.1:n.568+699T>A
XR_927073.2:n.711+699T>A
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