Canonical Allele Identifier: CA836195663
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1185456785
gnomAD v3: 7-17285399-A-C
gnomAD v4: 7-17285399-A-C
MyVariant Identifiers: chr7:g.17325023A>C (hg19) chr7:g.17285399A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285399A>C , CM000669.2:g.17285399A>C GRCh38
NC_000007.13:g.17325023A>C , CM000669.1:g.17325023A>C GRCh37
NC_000007.12:g.17291548A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10898A>C ENSP00000495987.1:n.-202-10898A>C
XR_927069.1:n.567+844T>G
XR_927070.1:n.567+844T>G
XR_927071.1:n.567+844T>G
XR_927072.1:n.568+844T>G
XR_927073.2:n.711+844T>G
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