Canonical Allele Identifier: CA1691255569
Community Standard Title: NC_000007.14:g.17244953T=
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244953T= , CM000669.2:g.17244953T= GRCh38
NC_000007.13:g.17284577T= , CM000669.1:g.17284577T= GRCh37
NC_000007.12:g.17251102T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-955-2021T= ENSP00000495987.1:n.-955-2021T=
XR_927073.2:n.861+14299A=