Canonical Allele Identifier: CA2681911122
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298519_17298581del , CM000669.2:g.17298519_17298581del GRCh38
NC_000007.13:g.17338143_17338205del , CM000669.1:g.17338143_17338205del GRCh37
NC_000007.12:g.17304668_17304730del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1895_20+1957del ENSP00000495987.1:n.20+1895_20+1957del