Canonical Allele Identifier: CA2511746318
Gene: AHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285415_17285416insCAAGA , CM000669.2:g.17285415_17285416insCAAGA GRCh38
NC_000007.13:g.17325039_17325040insCAAGA , CM000669.1:g.17325039_17325040insCAAGA GRCh37
NC_000007.12:g.17291564_17291565insCAAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10882_-202-10881insCAAGA ENSP00000495987.1:n.-202-10882_-202-10881insCAAGA
XR_927069.1:n.567+828_567+829insCTTGT
XR_927070.1:n.567+828_567+829insCTTGT
XR_927071.1:n.567+828_567+829insCTTGT
XR_927072.1:n.568+828_568+829insCTTGT
XR_927073.2:n.711+828_711+829insCTTGT
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