Canonical Allele Identifier: CA1691303615
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298424_17298426delinsTAA , CM000669.2:g.17298424_17298426delinsTAA GRCh38
NC_000007.13:g.17338048_17338050delinsTAA , CM000669.1:g.17338048_17338050delinsTAA GRCh37
NC_000007.12:g.17304573_17304575delinsTAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1800_20+1802delinsTAA ENSP00000495987.1:n.20+1800_20+1802delinsTAA
XR_927069.1:n.111_113delinsTTA
XR_927070.1:n.111_113delinsTTA
XR_927071.1:n.111_113delinsTTA
XR_927072.1:n.112_114delinsTTA
XR_927073.1:n.113_115delinsTTA
XR_927073.2:n.113_115delinsTTA