Canonical Allele Identifier: CA1098893970

Gene: AHR

Linked Data

• dbSNP Id: rs1781753266
• gnomAD v3: 7-17285515-G-C
• gnomAD v4: 7-17285515-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285515G>C , CM000669.2:g.17285515G>C	GRCh38
NC_000007.13:g.17325139G>C , CM000669.1:g.17325139G>C	GRCh37
NC_000007.12:g.17291664G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-10782G>C	ENSP00000495987.1:n.-202-10782G>C
XR_927069.1:n.567+728C>G
XR_927070.1:n.567+728C>G
XR_927071.1:n.567+728C>G
XR_927072.1:n.568+728C>G
XR_927073.2:n.711+728C>G