Canonical Allele Identifier: CA2681911157
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298542-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298542G>T , CM000669.2:g.17298542G>T GRCh38
NC_000007.13:g.17338166G>T , CM000669.1:g.17338166G>T GRCh37
NC_000007.12:g.17304691G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1918G>T ENSP00000495987.1:n.20+1918G>T
Search 100 bp 5'
Search 100 bp 3'