Canonical Allele Identifier: CA836200046

Gene: AHR

Linked Data

• dbSNP Id: rs10250822
• MyVariant Identifiers: chr7:g.17332989C>G (hg19) ; chr7:g.17293365C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293365C>G , CM000669.2:g.17293365C>G	GRCh38
NC_000007.13:g.17332989C>G , CM000669.1:g.17332989C>G	GRCh37
NC_000007.12:g.17299514C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-2932C>G	ENSP00000495987.1:n.-202-2932C>G
XR_927069.1:n.293+1801G>C
XR_927070.1:n.293+1801G>C
XR_927071.1:n.293+1801G>C
XR_927072.1:n.294+1801G>C
XR_927073.1:n.295+1801G>C
XR_927073.2:n.295+1801G>C