Canonical Allele Identifier: CA2774555329
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293513G>T , CM000669.2:g.17293513G>T GRCh38
NC_000007.13:g.17333137G>T , CM000669.1:g.17333137G>T GRCh37
NC_000007.12:g.17299662G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2784G>T ENSP00000495987.1:n.-202-2784G>T
XR_927069.1:n.293+1653C>A
XR_927070.1:n.293+1653C>A
XR_927071.1:n.293+1653C>A
XR_927072.1:n.294+1653C>A
XR_927073.1:n.295+1653C>A
XR_927073.2:n.295+1653C>A