Canonical Allele Identifier: CA573132034

Gene: AHR

Linked Data

• dbSNP Id: rs1210171572
• gnomAD v2: 7-17332946-C-T
• gnomAD v3: 7-17293322-C-T
• gnomAD v4: 7-17293322-C-T
• MyVariant Identifiers: chr7:g.17332946C>T (hg19) ; chr7:g.17293322C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293322C>T , CM000669.2:g.17293322C>T	GRCh38
NC_000007.13:g.17332946C>T , CM000669.1:g.17332946C>T	GRCh37
NC_000007.12:g.17299471C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-2975C>T	ENSP00000495987.1:n.-202-2975C>T
XR_927069.1:n.293+1844G>A
XR_927070.1:n.293+1844G>A
XR_927071.1:n.293+1844G>A
XR_927072.1:n.294+1844G>A
XR_927073.1:n.295+1844G>A
XR_927073.2:n.295+1844G>A