Canonical Allele Identifier: CA1691258335
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781397317
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247556C>A , CM000669.2:g.17247556C>A GRCh38
NC_000007.13:g.17287180C>A , CM000669.1:g.17287180C>A GRCh37
NC_000007.12:g.17253705C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-373C>A ENSP00000495987.1:n.-373C>A
XR_927073.2:n.861+11696G>T
Search 100 bp 5'
Search 100 bp 3'