Canonical Allele Identifier: CA1098893965

Gene: AHR

Linked Data

• dbSNP Id: rs777679847
• gnomAD v3: 7-17285509-C-A
• gnomAD v4: 7-17285509-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285509C>A , CM000669.2:g.17285509C>A	GRCh38
NC_000007.13:g.17325133C>A , CM000669.1:g.17325133C>A	GRCh37
NC_000007.12:g.17291658C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-10788C>A	ENSP00000495987.1:n.-202-10788C>A
XR_927069.1:n.567+734G>T
XR_927070.1:n.567+734G>T
XR_927071.1:n.567+734G>T
XR_927072.1:n.568+734G>T
XR_927073.2:n.711+734G>T