Canonical Allele Identifier: CA1098892998

Gene: AHR

Linked Data

• dbSNP Id: rs1781369001
• gnomAD v3: 7-17244914-C-T
• gnomAD v4: 7-17244914-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17244914C>T , CM000669.2:g.17244914C>T	GRCh38
NC_000007.13:g.17284538C>T , CM000669.1:g.17284538C>T	GRCh37
NC_000007.12:g.17251063C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-955-2060C>T	ENSP00000495987.1:n.-955-2060C>T
XR_927073.2:n.861+14338G>A