Canonical Allele Identifier: CA1098896340

Gene: AHR

Linked Data

• dbSNP Id: rs1781835013

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293132_17293134del , CM000669.2:g.17293132_17293134del	GRCh38
NC_000007.13:g.17332756_17332758del , CM000669.1:g.17332756_17332758del	GRCh37
NC_000007.12:g.17299281_17299283del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-3165_-202-3163del	ENSP00000495987.1:n.-202-3165_-202-3163del
XR_927069.1:n.293+2033_293+2035del
XR_927070.1:n.293+2033_293+2035del
XR_927071.1:n.293+2033_293+2035del
XR_927072.1:n.294+2033_294+2035del
XR_927073.1:n.296-1762_296-1760del
XR_927073.2:n.296-1762_296-1760del