Canonical Allele Identifier: CA454049406
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298432-C-G
MyVariant Identifiers: chr7:g.17338056C>G (hg19)

Genomic Alleles

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

Transcript Alleles

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