Canonical Allele Identifier: CA2713951975
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs2115321921

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269580T>C , CM000669.2:g.17269580T>C GRCh38
NC_000007.13:g.17309204T>C , CM000669.1:g.17309204T>C GRCh37
NC_000007.12:g.17275729T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-203+21854T>C ENSP00000495987.1:n.-203+21854T>C
XR_927073.2:n.785-10252A>G