Canonical Allele Identifier: CA2681911136
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298526-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298526A>C , CM000669.2:g.17298526A>C GRCh38
NC_000007.13:g.17338150A>C , CM000669.1:g.17338150A>C GRCh37
NC_000007.12:g.17304675A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1902A>C ENSP00000495987.1:n.20+1902A>C
XR_927069.1:n.11T>G
XR_927070.1:n.11T>G
XR_927071.1:n.11T>G
XR_927072.1:n.12T>G
XR_927073.1:n.13T>G
XR_927073.2:n.13T>G