Canonical Allele Identifier: CA2499639784
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285413_17285414insGTATATT , CM000669.2:g.17285413_17285414insGTATATT GRCh38
NC_000007.13:g.17325037_17325038insGTATATT , CM000669.1:g.17325037_17325038insGTATATT GRCh37
NC_000007.12:g.17291562_17291563insGTATATT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10884_-202-10883insGTATATT ENSP00000495987.1:n.-202-10884_-202-10883insGTATATT
XR_927069.1:n.567+829_567+830insAATATAC
XR_927070.1:n.567+829_567+830insAATATAC
XR_927071.1:n.567+829_567+830insAATATAC
XR_927072.1:n.568+829_568+830insAATATAC
XR_927073.2:n.711+829_711+830insAATATAC