Canonical Allele Identifier: CA454049373
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17338050A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298426A>T , CM000669.2:g.17298426A>T GRCh38
NC_000007.13:g.17338050A>T , CM000669.1:g.17338050A>T GRCh37
NC_000007.12:g.17304575A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.20+1802A>T ENSP00000495987.1:n.20+1802A>T
XR_927069.1:n.111T>A
XR_927070.1:n.111T>A
XR_927071.1:n.111T>A
XR_927072.1:n.112T>A
XR_927073.1:n.113T>A
XR_927073.2:n.113T>A