Canonical Allele Identifier: CA1098889111
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781588589
gnomAD v3: 7-17269567-T-G
gnomAD v4: 7-17269567-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269567T>G , CM000669.2:g.17269567T>G GRCh38
NC_000007.13:g.17309191T>G , CM000669.1:g.17309191T>G GRCh37
NC_000007.12:g.17275716T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21841T>G ENSP00000495987.1:n.-203+21841T>G
XR_927073.2:n.785-10239A>C