Canonical Allele Identifier: CA1691291801
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285521A= , CM000669.2:g.17285521A= GRCh38
NC_000007.13:g.17325145A= , CM000669.1:g.17325145A= GRCh37
NC_000007.12:g.17291670A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10776A= ENSP00000495987.1:n.-202-10776A=
XR_927069.1:n.567+722T=
XR_927070.1:n.567+722T=
XR_927071.1:n.567+722T=
XR_927072.1:n.568+722T=
XR_927073.2:n.711+722T=