Canonical Allele Identifier: CA2713955422
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs2115307359

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247570A>C , CM000669.2:g.17247570A>C GRCh38
NC_000007.13:g.17287194A>C , CM000669.1:g.17287194A>C GRCh37
NC_000007.12:g.17253719A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-359A>C ENSP00000495987.1:n.-359A>C
XR_927073.2:n.861+11682T>G