Canonical Allele Identifier: CA1098896373

Gene: AHR

Linked Data

• dbSNP Id: rs1781836271
• gnomAD v3: 7-17293293-T-G
• gnomAD v4: 7-17293293-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293293T>G , CM000669.2:g.17293293T>G	GRCh38
NC_000007.13:g.17332917T>G , CM000669.1:g.17332917T>G	GRCh37
NC_000007.12:g.17299442T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-3004T>G	ENSP00000495987.1:n.-202-3004T>G
XR_927069.1:n.293+1873A>C
XR_927070.1:n.293+1873A>C
XR_927071.1:n.293+1873A>C
XR_927072.1:n.294+1873A>C
XR_927073.1:n.295+1873A>C
XR_927073.2:n.295+1873A>C