Canonical Allele Identifier: CA1691291816

Gene: AHR

Linked Data

• dbSNP Id: rs1781753432

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285533C>A , CM000669.2:g.17285533C>A	GRCh38
NC_000007.13:g.17325157C>A , CM000669.1:g.17325157C>A	GRCh37
NC_000007.12:g.17291682C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-10764C>A	ENSP00000495987.1:n.-202-10764C>A
XR_927069.1:n.567+710G>T
XR_927070.1:n.567+710G>T
XR_927071.1:n.567+710G>T
XR_927072.1:n.568+710G>T
XR_927073.2:n.711+710G>T