Canonical Allele Identifier: CA154826859
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs570398266
gnomAD v3: 7-17285510-G-A
gnomAD v4: 7-17285510-G-A
MyVariant Identifiers: chr7:g.17325134G>A (hg19) chr7:g.17285510G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285510G>A , CM000669.2:g.17285510G>A GRCh38
NC_000007.13:g.17325134G>A , CM000669.1:g.17325134G>A GRCh37
NC_000007.12:g.17291659G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-10787G>A ENSP00000495987.1:n.-202-10787G>A
XR_927069.1:n.567+733C>T
XR_927070.1:n.567+733C>T
XR_927071.1:n.567+733C>T
XR_927072.1:n.568+733C>T
XR_927073.2:n.711+733C>T
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