Canonical Allele Identifier: CA836200144

Gene: AHR

Linked Data

• dbSNP Id: rs1280359287
• gnomAD v3: 7-17293527-AGCTAAATTCTTGTAAT-A
• gnomAD v4: 7-17293527-AGCTAAATTCTTGTAAT-A
• MyVariant Identifiers: chr7:g.17333152_17333167del (hg19) ; chr7:g.17293528_17293543del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293530_17293545del , CM000669.2:g.17293530_17293545del	GRCh38
NC_000007.13:g.17333154_17333169del , CM000669.1:g.17333154_17333169del	GRCh37
NC_000007.12:g.17299679_17299694del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-2767_-202-2752del	ENSP00000495987.1:n.-202-2767_-202-2752del
XR_927069.1:n.293+1623_293+1638del
XR_927070.1:n.293+1623_293+1638del
XR_927071.1:n.293+1623_293+1638del
XR_927072.1:n.294+1623_294+1638del
XR_927073.1:n.295+1623_295+1638del
XR_927073.2:n.295+1623_295+1638del