Canonical Allele Identifier: CA2681911138
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298527-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298527A>T , CM000669.2:g.17298527A>T GRCh38
NC_000007.13:g.17338151A>T , CM000669.1:g.17338151A>T GRCh37
NC_000007.12:g.17304676A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1903A>T ENSP00000495987.1:n.20+1903A>T
XR_927069.1:n.10T>A
XR_927070.1:n.10T>A
XR_927071.1:n.10T>A
XR_927072.1:n.11T>A
XR_927073.1:n.12T>A
XR_927073.2:n.12T>A