Canonical Allele Identifier: CA2542660885
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269562G>C , CM000669.2:g.17269562G>C GRCh38
NC_000007.13:g.17309186G>C , CM000669.1:g.17309186G>C GRCh37
NC_000007.12:g.17275711G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21836G>C ENSP00000495987.1:n.-203+21836G>C
XR_927073.2:n.785-10234C>G