Canonical Allele Identifier: CA1691291858
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781754323

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285599A>T , CM000669.2:g.17285599A>T GRCh38
NC_000007.13:g.17325223A>T , CM000669.1:g.17325223A>T GRCh37
NC_000007.12:g.17291748A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10698A>T ENSP00000495987.1:n.-202-10698A>T
XR_927069.1:n.567+644T>A
XR_927070.1:n.567+644T>A
XR_927071.1:n.567+644T>A
XR_927072.1:n.568+644T>A
XR_927073.2:n.711+644T>A