Canonical Allele Identifier: CA2681907549
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17247546-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247546A>G , CM000669.2:g.17247546A>G GRCh38
NC_000007.13:g.17287170A>G , CM000669.1:g.17287170A>G GRCh37
NC_000007.12:g.17253695A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-383A>G ENSP00000495987.1:n.-383A>G
XR_927073.2:n.861+11706T>C