Canonical Allele Identifier: CA1098894240
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781397180
gnomAD v3: 7-17247548-A-G
gnomAD v4: 7-17247548-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247548A>G , CM000669.2:g.17247548A>G GRCh38
NC_000007.13:g.17287172A>G , CM000669.1:g.17287172A>G GRCh37
NC_000007.12:g.17253697A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-381A>G ENSP00000495987.1:n.-381A>G
XR_927073.2:n.861+11704T>C