Canonical Allele Identifier: CA1691291799
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285516T= , CM000669.2:g.17285516T= GRCh38
NC_000007.13:g.17325140T= , CM000669.1:g.17325140T= GRCh37
NC_000007.12:g.17291665T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10781T= ENSP00000495987.1:n.-202-10781T=
XR_927069.1:n.567+727A=
XR_927070.1:n.567+727A=
XR_927071.1:n.567+727A=
XR_927072.1:n.568+727A=
XR_927073.2:n.711+727A=