Canonical Allele Identifier: CA1691291812
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1584020004

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285531T>C , CM000669.2:g.17285531T>C GRCh38
NC_000007.13:g.17325155T>C , CM000669.1:g.17325155T>C GRCh37
NC_000007.12:g.17291680T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10766T>C ENSP00000495987.1:n.-202-10766T>C
XR_927069.1:n.567+712A>G
XR_927070.1:n.567+712A>G
XR_927071.1:n.567+712A>G
XR_927072.1:n.568+712A>G
XR_927073.2:n.711+712A>G