Canonical Allele Identifier: CA836234351

Gene: AHR

Linked Data

• dbSNP Id: rs4489213
• MyVariant Identifiers: chr7:g.17309180G>T (hg19) ; chr7:g.17269556G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17269556G>T , CM000669.2:g.17269556G>T	GRCh38
NC_000007.13:g.17309180G>T , CM000669.1:g.17309180G>T	GRCh37
NC_000007.12:g.17275705G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-203+21830G>T	ENSP00000495987.1:n.-203+21830G>T
XR_927073.2:n.785-10228C>A