Canonical Allele Identifier: CA1691258341
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781397415

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247567del , CM000669.2:g.17247567del GRCh38
NC_000007.13:g.17287191del , CM000669.1:g.17287191del GRCh37
NC_000007.12:g.17253716del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-362del ENSP00000495987.1:n.-362del
XR_927073.2:n.861+11685del