Canonical Allele Identifier: CA2681907562
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17247566-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247566A>G , CM000669.2:g.17247566A>G GRCh38
NC_000007.13:g.17287190A>G , CM000669.1:g.17287190A>G GRCh37
NC_000007.12:g.17253715A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-363A>G ENSP00000495987.1:n.-363A>G
XR_927073.2:n.861+11686T>C