Canonical Allele Identifier: CA454049382
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298428-T-A
MyVariant Identifiers: chr7:g.17338052T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298428T>A , CM000669.2:g.17298428T>A GRCh38
NC_000007.13:g.17338052T>A , CM000669.1:g.17338052T>A GRCh37
NC_000007.12:g.17304577T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.20+1804T>A ENSP00000495987.1:n.20+1804T>A
XR_927069.1:n.109A>T
XR_927070.1:n.109A>T
XR_927071.1:n.109A>T
XR_927072.1:n.110A>T
XR_927073.1:n.111A>T
XR_927073.2:n.111A>T