Canonical Allele Identifier: CA1098896518
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781838663

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293511del , CM000669.2:g.17293511del GRCh38
NC_000007.13:g.17333135del , CM000669.1:g.17333135del GRCh37
NC_000007.12:g.17299660del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-2786del ENSP00000495987.1:n.-202-2786del
XR_927069.1:n.293+1655del
XR_927070.1:n.293+1655del
XR_927071.1:n.293+1655del
XR_927072.1:n.294+1655del
XR_927073.1:n.295+1655del
XR_927073.2:n.295+1655del