Canonical Allele Identifier: CA1691290793
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781588628

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269571T>C , CM000669.2:g.17269571T>C GRCh38
NC_000007.13:g.17309195T>C , CM000669.1:g.17309195T>C GRCh37
NC_000007.12:g.17275720T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-203+21845T>C ENSP00000495987.1:n.-203+21845T>C
XR_927073.2:n.785-10243A>G