Canonical Allele Identifier: CA1691255520
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781368908

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244896T>C , CM000669.2:g.17244896T>C GRCh38
NC_000007.13:g.17284520T>C , CM000669.1:g.17284520T>C GRCh37
NC_000007.12:g.17251045T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2078T>C ENSP00000495987.1:n.-955-2078T>C
XR_927073.2:n.861+14356A>G