Canonical Allele Identifier: CA2713879027
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781369139

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244937C>G , CM000669.2:g.17244937C>G GRCh38
NC_000007.13:g.17284561C>G , CM000669.1:g.17284561C>G GRCh37
NC_000007.12:g.17251086C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2037C>G ENSP00000495987.1:n.-955-2037C>G
XR_927073.2:n.861+14315G>C