Canonical Allele Identifier: CA454049425
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781907570
gnomAD v3: 7-17298435-A-C
gnomAD v4: 7-17298435-A-C
MyVariant Identifiers: chr7:g.17338059A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298435A>C , CM000669.2:g.17298435A>C GRCh38
NC_000007.13:g.17338059A>C , CM000669.1:g.17338059A>C GRCh37
NC_000007.12:g.17304584A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1811A>C ENSP00000495987.1:n.20+1811A>C
XR_927069.1:n.102T>G
XR_927070.1:n.102T>G
XR_927071.1:n.102T>G
XR_927072.1:n.103T>G
XR_927073.1:n.104T>G
XR_927073.2:n.104T>G