Canonical Allele Identifier: CA1691291860
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285600A= , CM000669.2:g.17285600A= GRCh38
NC_000007.13:g.17325224A= , CM000669.1:g.17325224A= GRCh37
NC_000007.12:g.17291749A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10697A= ENSP00000495987.1:n.-202-10697A=
XR_927069.1:n.567+643T=
XR_927070.1:n.567+643T=
XR_927071.1:n.567+643T=
XR_927072.1:n.568+643T=
XR_927073.2:n.711+643T=