Canonical Allele Identifier: CA2681907552
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17247553-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247553C>A , CM000669.2:g.17247553C>A GRCh38
NC_000007.13:g.17287177C>A , CM000669.1:g.17287177C>A GRCh37
NC_000007.12:g.17253702C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-376C>A ENSP00000495987.1:n.-376C>A
XR_927073.2:n.861+11699G>T
Search 100 bp 5'
Search 100 bp 3'