Canonical Allele Identifier: CA454049418

Gene: AHR

Linked Data

• gnomAD v4: 7-17298434-T-A
• MyVariant Identifiers: chr7:g.17338058T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17298434T>A , CM000669.2:g.17298434T>A	GRCh38
NC_000007.13:g.17338058T>A , CM000669.1:g.17338058T>A	GRCh37
NC_000007.12:g.17304583T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.20+1810T>A	ENSP00000495987.1:n.20+1810T>A
XR_927069.1:n.103A>T
XR_927070.1:n.103A>T
XR_927071.1:n.103A>T
XR_927072.1:n.104A>T
XR_927073.1:n.105A>T
XR_927073.2:n.105A>T