Canonical Allele Identifier: CA154826853

Gene: AHR

Linked Data

• dbSNP Id: rs575253167
• gnomAD v3: 7-17285474-G-A
• gnomAD v4: 7-17285474-G-A
• MyVariant Identifiers: chr7:g.17325098G>A (hg19) ; chr7:g.17285474G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285474G>A , CM000669.2:g.17285474G>A	GRCh38
NC_000007.13:g.17325098G>A , CM000669.1:g.17325098G>A	GRCh37
NC_000007.12:g.17291623G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-10823G>A	ENSP00000495987.1:n.-202-10823G>A
XR_927069.1:n.567+769C>T
XR_927070.1:n.567+769C>T
XR_927071.1:n.567+769C>T
XR_927072.1:n.568+769C>T
XR_927073.2:n.711+769C>T