Canonical Allele Identifier: CA154826858

Gene: AHR

Linked Data

• dbSNP Id: rs777679847
• gnomAD v2: 7-17325133-C-T
• gnomAD v3: 7-17285509-C-T
• gnomAD v4: 7-17285509-C-T
• MyVariant Identifiers: chr7:g.17325133C>T (hg19) ; chr7:g.17285509C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285509C>T , CM000669.2:g.17285509C>T	GRCh38
NC_000007.13:g.17325133C>T , CM000669.1:g.17325133C>T	GRCh37
NC_000007.12:g.17291658C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-10788C>T	ENSP00000495987.1:n.-202-10788C>T
XR_927069.1:n.567+734G>A
XR_927070.1:n.567+734G>A
XR_927071.1:n.567+734G>A
XR_927072.1:n.568+734G>A
XR_927073.2:n.711+734G>A