Canonical Allele Identifier: CA1691291864
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285602_17285603delinsAT , CM000669.2:g.17285602_17285603delinsAT GRCh38
NC_000007.13:g.17325226_17325227delinsAT , CM000669.1:g.17325226_17325227delinsAT GRCh37
NC_000007.12:g.17291751_17291752delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10695_-202-10694delinsAT ENSP00000495987.1:n.-202-10695_-202-10694...
XR_927069.1:n.567+640_567+641delinsAT
XR_927070.1:n.567+640_567+641delinsAT
XR_927071.1:n.567+640_567+641delinsAT
XR_927072.1:n.568+640_568+641delinsAT
XR_927073.2:n.711+640_711+641delinsAT