Canonical Allele Identifier: CA1691303886
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298533T= , CM000669.2:g.17298533T= GRCh38
NC_000007.13:g.17338157T= , CM000669.1:g.17338157T= GRCh37
NC_000007.12:g.17304682T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1909T= ENSP00000495987.1:n.20+1909T=
XR_927069.1:n.4A=
XR_927070.1:n.4A=
XR_927071.1:n.4A=
XR_927072.1:n.5A=
XR_927073.1:n.6A=
XR_927073.2:n.6A=