Canonical Allele Identifier: CA836200096

Gene: AHR

Linked Data

• dbSNP Id: rs1365451246
• MyVariant Identifiers: chr7:g.17333028G>C (hg19) ; chr7:g.17293404G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293404G>C , CM000669.2:g.17293404G>C	GRCh38
NC_000007.13:g.17333028G>C , CM000669.1:g.17333028G>C	GRCh37
NC_000007.12:g.17299553G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-2893G>C	ENSP00000495987.1:n.-202-2893G>C
XR_927069.1:n.293+1762C>G
XR_927070.1:n.293+1762C>G
XR_927071.1:n.293+1762C>G
XR_927072.1:n.294+1762C>G
XR_927073.1:n.295+1762C>G
XR_927073.2:n.295+1762C>G