Canonical Allele Identifier: CA2527063496
Gene: AHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285514G>T , CM000669.2:g.17285514G>T GRCh38
NC_000007.13:g.17325138G>T , CM000669.1:g.17325138G>T GRCh37
NC_000007.12:g.17291663G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10783G>T ENSP00000495987.1:n.-202-10783G>T
XR_927069.1:n.567+729C>A
XR_927070.1:n.567+729C>A
XR_927071.1:n.567+729C>A
XR_927072.1:n.568+729C>A
XR_927073.2:n.711+729C>A