Canonical Allele Identifier: CA836218812

Gene: AHR

Linked Data

• dbSNP Id: rs1289509236
• MyVariant Identifiers: chr7:g.17284524A>T (hg19) ; chr7:g.17244900A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17244900A>T , CM000669.2:g.17244900A>T	GRCh38
NC_000007.13:g.17284524A>T , CM000669.1:g.17284524A>T	GRCh37
NC_000007.12:g.17251049A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-955-2074A>T	ENSP00000495987.1:n.-955-2074A>T
XR_927073.2:n.861+14352T>A