Canonical Allele Identifier: CA1691291718

Gene: AHR

Linked Data

• dbSNP Id: rs1781752248

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285417A>T , CM000669.2:g.17285417A>T	GRCh38
NC_000007.13:g.17325041A>T , CM000669.1:g.17325041A>T	GRCh37
NC_000007.12:g.17291566A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-10880A>T	ENSP00000495987.1:n.-202-10880A>T
XR_927069.1:n.567+826T>A
XR_927070.1:n.567+826T>A
XR_927071.1:n.567+826T>A
XR_927072.1:n.568+826T>A
XR_927073.2:n.711+826T>A