Canonical Allele Identifier: CA917954503
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1584013913

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269594_17269609del , CM000669.2:g.17269594_17269609del GRCh38
NC_000007.13:g.17309218_17309233del , CM000669.1:g.17309218_17309233del GRCh37
NC_000007.12:g.17275743_17275758del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21868_-203+21883del ENSP00000495987.1:n.-203+21868_-203+21883del
XR_927073.2:n.785-10278_785-10263del