Canonical Allele Identifier: CA1098896532

Gene: AHR

Linked Data

• dbSNP Id: rs1781842495
• gnomAD v3: 7-17293566-T-C
• gnomAD v4: 7-17293566-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293566T>C , CM000669.2:g.17293566T>C	GRCh38
NC_000007.13:g.17333190T>C , CM000669.1:g.17333190T>C	GRCh37
NC_000007.12:g.17299715T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-2731T>C	ENSP00000495987.1:n.-202-2731T>C
XR_927069.1:n.293+1600A>G
XR_927070.1:n.293+1600A>G
XR_927071.1:n.293+1600A>G
XR_927072.1:n.294+1600A>G
XR_927073.1:n.295+1600A>G
XR_927073.2:n.295+1600A>G