Canonical Allele Identifier: CA1691291731
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285438_17285442delinsTAAAG , CM000669.2:g.17285438_17285442delinsTAAAG GRCh38
NC_000007.13:g.17325062_17325066delinsTAAAG , CM000669.1:g.17325062_17325066delinsTAAAG GRCh37
NC_000007.12:g.17291587_17291591delinsTAAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10859_-202-10855delinsTAAAG ENSP00000495987.1:n.-202-10859_-202-10855delinsTAAAG
XR_927069.1:n.567+801_567+805delinsCTTTA
XR_927070.1:n.567+801_567+805delinsCTTTA
XR_927071.1:n.567+801_567+805delinsCTTTA
XR_927072.1:n.568+801_568+805delinsCTTTA
XR_927073.2:n.711+801_711+805delinsCTTTA
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