Canonical Allele Identifier: CA1691298799

Gene: AHR

Linked Data

• dbSNP Id: rs1781836399

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293302C>G , CM000669.2:g.17293302C>G	GRCh38
NC_000007.13:g.17332926C>G , CM000669.1:g.17332926C>G	GRCh37
NC_000007.12:g.17299451C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-2995C>G	ENSP00000495987.1:n.-202-2995C>G
XR_927069.1:n.293+1864G>C
XR_927070.1:n.293+1864G>C
XR_927071.1:n.293+1864G>C
XR_927072.1:n.294+1864G>C
XR_927073.1:n.295+1864G>C
XR_927073.2:n.295+1864G>C