Canonical Allele Identifier: CA2541729290
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285575G>A , CM000669.2:g.17285575G>A GRCh38
NC_000007.13:g.17325199G>A , CM000669.1:g.17325199G>A GRCh37
NC_000007.12:g.17291724G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10722G>A ENSP00000495987.1:n.-202-10722G>A
XR_927069.1:n.567+668C>T
XR_927070.1:n.567+668C>T
XR_927071.1:n.567+668C>T
XR_927072.1:n.568+668C>T
XR_927073.2:n.711+668C>T