Canonical Allele Identifier: CA1691255506
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1487461836

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244866G>T , CM000669.2:g.17244866G>T GRCh38
NC_000007.13:g.17284490G>T , CM000669.1:g.17284490G>T GRCh37
NC_000007.12:g.17251015G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2108G>T ENSP00000495987.1:n.-955-2108G>T
XR_927073.2:n.861+14386C>A