Canonical Allele Identifier: CA154822092
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1044735997
gnomAD v2: 7-17284528-T-A
gnomAD v3: 7-17244904-T-A
gnomAD v4: 7-17244904-T-A
MyVariant Identifiers: chr7:g.17284528T>A (hg19) chr7:g.17244904T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244904T>A , CM000669.2:g.17244904T>A GRCh38
NC_000007.13:g.17284528T>A , CM000669.1:g.17284528T>A GRCh37
NC_000007.12:g.17251053T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2070T>A ENSP00000495987.1:n.-955-2070T>A
XR_927073.2:n.861+14348A>T
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