Canonical Allele Identifier: CA154826865
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1007084012

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285558_17285559del , CM000669.2:g.17285558_17285559del GRCh38
NC_000007.13:g.17325182_17325183del , CM000669.1:g.17325182_17325183del GRCh37
NC_000007.12:g.17291707_17291708del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10739_-202-10738del ENSP00000495987.1:n.-202-10739_-202-10738...
XR_927069.1:n.567+685_567+686del
XR_927070.1:n.567+685_567+686del
XR_927071.1:n.567+685_567+686del
XR_927072.1:n.568+685_568+686del
XR_927073.2:n.711+685_711+686del