Canonical Allele Identifier: CA836203368
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1410869595
gnomAD v3: 7-17298527-A-C
gnomAD v4: 7-17298527-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298527A>C , CM000669.2:g.17298527A>C GRCh38
NC_000007.13:g.17338151A>C , CM000669.1:g.17338151A>C GRCh37
NC_000007.12:g.17304676A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1903A>C ENSP00000495987.1:n.20+1903A>C
XR_927069.1:n.10T>G
XR_927070.1:n.10T>G
XR_927071.1:n.10T>G
XR_927072.1:n.11T>G
XR_927073.1:n.12T>G
XR_927073.2:n.12T>G