Canonical Allele Identifier: CA836200076
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1430347190

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293397G>T , CM000669.2:g.17293397G>T GRCh38
NC_000007.13:g.17333021G>T , CM000669.1:g.17333021G>T GRCh37
NC_000007.12:g.17299546G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2900G>T ENSP00000495987.1:n.-202-2900G>T
XR_927069.1:n.293+1769C>A
XR_927070.1:n.293+1769C>A
XR_927071.1:n.293+1769C>A
XR_927072.1:n.294+1769C>A
XR_927073.1:n.295+1769C>A
XR_927073.2:n.295+1769C>A