Canonical Allele Identifier: CA2681911146
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298533-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298533T>A , CM000669.2:g.17298533T>A GRCh38
NC_000007.13:g.17338157T>A , CM000669.1:g.17338157T>A GRCh37
NC_000007.12:g.17304682T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1909T>A ENSP00000495987.1:n.20+1909T>A
XR_927069.1:n.4A>T
XR_927070.1:n.4A>T
XR_927071.1:n.4A>T
XR_927072.1:n.5A>T
XR_927073.1:n.6A>T
XR_927073.2:n.6A>T