Canonical Allele Identifier: CA1098898556
Gene: AHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298467_17298594del , CM000669.2:g.17298467_17298594del GRCh38
NC_000007.13:g.17338091_17338218del , CM000669.1:g.17338091_17338218del GRCh37
NC_000007.12:g.17304616_17304743del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1843_20+1970del ENSP00000495987.1:n.20+1843_20+1970del