Canonical Allele Identifier: CA1098896416
Gene: AHR HGNC NCBI

Linked Data

gnomAD v3: 7-17293304-A-T
gnomAD v4: 7-17293304-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293304A>T , CM000669.2:g.17293304A>T GRCh38
NC_000007.13:g.17332928A>T , CM000669.1:g.17332928A>T GRCh37
NC_000007.12:g.17299453A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2993A>T ENSP00000495987.1:n.-202-2993A>T
XR_927069.1:n.293+1862T>A
XR_927070.1:n.293+1862T>A
XR_927071.1:n.293+1862T>A
XR_927072.1:n.294+1862T>A
XR_927073.1:n.295+1862T>A
XR_927073.2:n.295+1862T>A