Canonical Allele Identifier: CA573132790
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1285545082
gnomAD v2: 7-17338160-A-G
gnomAD v3: 7-17298536-A-G
gnomAD v4: 7-17298536-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298536A>G , CM000669.2:g.17298536A>G GRCh38
NC_000007.13:g.17338160A>G , CM000669.1:g.17338160A>G GRCh37
NC_000007.12:g.17304685A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1912A>G ENSP00000495987.1:n.20+1912A>G
XR_927069.1:n.1T>C
XR_927070.1:n.1T>C
XR_927071.1:n.1T>C
XR_927072.1:n.2T>C
XR_927073.1:n.3T>C
XR_927073.2:n.3T>C