Canonical Allele Identifier: CA1691298782

Gene: AHR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293288_17293290delinsCTT , CM000669.2:g.17293288_17293290delinsCTT	GRCh38
NC_000007.13:g.17332912_17332914delinsCTT , CM000669.1:g.17332912_17332914delinsCTT	GRCh37
NC_000007.12:g.17299437_17299439delinsCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-3009_-202-3007delinsCTT	ENSP00000495987.1:n.-202-3009_-202-3007delinsCTT
XR_927069.1:n.293+1876_293+1878delinsAAG
XR_927070.1:n.293+1876_293+1878delinsAAG
XR_927071.1:n.293+1876_293+1878delinsAAG
XR_927072.1:n.294+1876_294+1878delinsAAG
XR_927073.1:n.295+1876_295+1878delinsAAG
XR_927073.2:n.295+1876_295+1878delinsAAG