Canonical Allele Identifier: CA454049404
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17338056C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298432C>A , CM000669.2:g.17298432C>A GRCh38
NC_000007.13:g.17338056C>A , CM000669.1:g.17338056C>A GRCh37
NC_000007.12:g.17304581C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.20+1808C>A ENSP00000495987.1:n.20+1808C>A
XR_927069.1:n.105G>T
XR_927070.1:n.105G>T
XR_927071.1:n.105G>T
XR_927072.1:n.106G>T
XR_927073.1:n.107G>T
XR_927073.2:n.107G>T