Canonical Allele Identifier: CA2681907554

Gene: AHR

Linked Data

• gnomAD v4: 7-17247553-C-T

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-376C>T	ENSP00000495987.1:n.-376C>T
XR_927073.2:n.861+11699G>A