Canonical Allele Identifier: CA154828325
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1043591690
gnomAD v4: 7-17298525-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298525G>A , CM000669.2:g.17298525G>A GRCh38
NC_000007.13:g.17338149G>A , CM000669.1:g.17338149G>A GRCh37
NC_000007.12:g.17304674G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1901G>A ENSP00000495987.1:n.20+1901G>A
XR_927069.1:n.12C>T
XR_927070.1:n.12C>T
XR_927071.1:n.12C>T
XR_927072.1:n.13C>T
XR_927073.1:n.14C>T
XR_927073.2:n.14C>T