Canonical Allele Identifier: CA1691303876
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298528T= , CM000669.2:g.17298528T= GRCh38
NC_000007.13:g.17338152T= , CM000669.1:g.17338152T= GRCh37
NC_000007.12:g.17304677T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1904T= ENSP00000495987.1:n.20+1904T=
XR_927069.1:n.9A=
XR_927070.1:n.9A=
XR_927071.1:n.9A=
XR_927072.1:n.10A=
XR_927073.1:n.11A=
XR_927073.2:n.11A=