Canonical Allele Identifier: CA2774568183
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269582C>G , CM000669.2:g.17269582C>G GRCh38
NC_000007.13:g.17309206C>G , CM000669.1:g.17309206C>G GRCh37
NC_000007.12:g.17275731C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21856C>G ENSP00000495987.1:n.-203+21856C>G
XR_927073.2:n.785-10254G>C