Canonical Allele Identifier: CA454049431
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs532703285
gnomAD v3: 7-17298436-T-A
gnomAD v4: 7-17298436-T-A
MyVariant Identifiers: chr7:g.17338060T>A (hg19) chr7:g.17298436T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298436T>A , CM000669.2:g.17298436T>A GRCh38
NC_000007.13:g.17338060T>A , CM000669.1:g.17338060T>A GRCh37
NC_000007.12:g.17304585T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.20+1812T>A ENSP00000495987.1:n.20+1812T>A
XR_927069.1:n.101A>T
XR_927070.1:n.101A>T
XR_927071.1:n.101A>T
XR_927072.1:n.102A>T
XR_927073.1:n.103A>T
XR_927073.2:n.103A>T
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