Canonical Allele Identifier: CA1098896348

Gene: AHR

Linked Data

• dbSNP Id: rs1781835476
• gnomAD v3: 7-17293184-G-A
• gnomAD v4: 7-17293184-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293184G>A , CM000669.2:g.17293184G>A	GRCh38
NC_000007.13:g.17332808G>A , CM000669.1:g.17332808G>A	GRCh37
NC_000007.12:g.17299333G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-3113G>A	ENSP00000495987.1:n.-202-3113G>A
XR_927069.1:n.293+1982C>T
XR_927070.1:n.293+1982C>T
XR_927071.1:n.293+1982C>T
XR_927072.1:n.294+1982C>T
XR_927073.1:n.296-1813C>T
XR_927073.2:n.296-1813C>T