Canonical Allele Identifier: CA454049380

Gene: AHR

Linked Data

• gnomAD v4: 7-17298428-T-G
• MyVariant Identifiers: chr7:g.17338052T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17298428T>G , CM000669.2:g.17298428T>G	GRCh38
NC_000007.13:g.17338052T>G , CM000669.1:g.17338052T>G	GRCh37
NC_000007.12:g.17304577T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.20+1804T>G	ENSP00000495987.1:n.20+1804T>G
XR_927069.1:n.109A>C
XR_927070.1:n.109A>C
XR_927071.1:n.109A>C
XR_927072.1:n.110A>C
XR_927073.1:n.111A>C
XR_927073.2:n.111A>C