Canonical Allele Identifier: CA2681911101
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298511_17298584del , CM000669.2:g.17298511_17298584del GRCh38
NC_000007.13:g.17338135_17338208del , CM000669.1:g.17338135_17338208del GRCh37
NC_000007.12:g.17304660_17304733del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1887_20+1960del ENSP00000495987.1:n.20+1887_20+1960del