Canonical Allele Identifier: CA2547861420
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293198G>T , CM000669.2:g.17293198G>T GRCh38
NC_000007.13:g.17332822G>T , CM000669.1:g.17332822G>T GRCh37
NC_000007.12:g.17299347G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-3099G>T ENSP00000495987.1:n.-202-3099G>T
XR_927069.1:n.293+1968C>A
XR_927070.1:n.293+1968C>A
XR_927071.1:n.293+1968C>A
XR_927072.1:n.294+1968C>A
XR_927073.1:n.296-1827C>A
XR_927073.2:n.296-1827C>A