Canonical Allele Identifier: CA836218778

Gene: AHR

Linked Data

• dbSNP Id: rs1443165214
• gnomAD v3: 7-17244859-C-G
• gnomAD v4: 7-17244859-C-G
• MyVariant Identifiers: chr7:g.17284483C>G (hg19) ; chr7:g.17244859C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17244859C>G , CM000669.2:g.17244859C>G	GRCh38
NC_000007.13:g.17284483C>G , CM000669.1:g.17284483C>G	GRCh37
NC_000007.12:g.17251008C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-955-2115C>G	ENSP00000495987.1:n.-955-2115C>G
XR_927073.2:n.861+14393G>C