Canonical Allele Identifier: CA2681911130
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298523-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298523C>A , CM000669.2:g.17298523C>A GRCh38
NC_000007.13:g.17338147C>A , CM000669.1:g.17338147C>A GRCh37
NC_000007.12:g.17304672C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1899C>A ENSP00000495987.1:n.20+1899C>A
XR_927069.1:n.14G>T
XR_927070.1:n.14G>T
XR_927071.1:n.14G>T
XR_927072.1:n.15G>T
XR_927073.1:n.16G>T
XR_927073.2:n.16G>T