Canonical Allele Identifier: CA573130684
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1266201342
gnomAD v2: 7-17325128-A-G
gnomAD v3: 7-17285504-A-G
gnomAD v4: 7-17285504-A-G
MyVariant Identifiers: chr7:g.17325128A>G (hg19) chr7:g.17285504A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285504A>G , CM000669.2:g.17285504A>G GRCh38
NC_000007.13:g.17325128A>G , CM000669.1:g.17325128A>G GRCh37
NC_000007.12:g.17291653A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10793A>G ENSP00000495987.1:n.-202-10793A>G
XR_927069.1:n.567+739T>C
XR_927070.1:n.567+739T>C
XR_927071.1:n.567+739T>C
XR_927072.1:n.568+739T>C
XR_927073.2:n.711+739T>C
Search 100 bp 5'
Search 100 bp 3'