Canonical Allele Identifier: CA1691291828
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285546_17285548delinsTAA , CM000669.2:g.17285546_17285548delinsTAA GRCh38
NC_000007.13:g.17325170_17325172delinsTAA , CM000669.1:g.17325170_17325172delinsTAA GRCh37
NC_000007.12:g.17291695_17291697delinsTAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10751_-202-10749delinsTAA ENSP00000495987.1:n.-202-10751_-202-10749...
XR_927069.1:n.567+695_567+697delinsTTA
XR_927070.1:n.567+695_567+697delinsTTA
XR_927071.1:n.567+695_567+697delinsTTA
XR_927072.1:n.568+695_568+697delinsTTA
XR_927073.2:n.711+695_711+697delinsTTA