Canonical Allele Identifier: CA1691291851
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1584020021

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285591T>A , CM000669.2:g.17285591T>A GRCh38
NC_000007.13:g.17325215T>A , CM000669.1:g.17325215T>A GRCh37
NC_000007.12:g.17291740T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10706T>A ENSP00000495987.1:n.-202-10706T>A
XR_927069.1:n.567+652A>T
XR_927070.1:n.567+652A>T
XR_927071.1:n.567+652A>T
XR_927072.1:n.568+652A>T
XR_927073.2:n.711+652A>T