Canonical Allele Identifier: CA1098893916

Gene: AHR

Linked Data

• dbSNP Id: rs1781752033
• gnomAD v3: 7-17285391-A-C
• gnomAD v4: 7-17285391-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285391A>C , CM000669.2:g.17285391A>C	GRCh38
NC_000007.13:g.17325015A>C , CM000669.1:g.17325015A>C	GRCh37
NC_000007.12:g.17291540A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-10906A>C	ENSP00000495987.1:n.-202-10906A>C
XR_927069.1:n.567+852T>G
XR_927070.1:n.567+852T>G
XR_927071.1:n.567+852T>G
XR_927072.1:n.568+852T>G
XR_927073.2:n.711+852T>G