Canonical Allele Identifier: CA1691290884
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs12670403
gnomAD v4: 7-17269655-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269655C>G , CM000669.2:g.17269655C>G GRCh38
NC_000007.13:g.17309279C>G , CM000669.1:g.17309279C>G GRCh37
NC_000007.12:g.17275804C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-203+21929C>G ENSP00000495987.1:n.-203+21929C>G
XR_927073.2:n.785-10327G>C