Canonical Allele Identifier: CA1098893000
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781369139
gnomAD v3: 7-17244937-C-A
gnomAD v4: 7-17244937-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244937C>A , CM000669.2:g.17244937C>A GRCh38
NC_000007.13:g.17284561C>A , CM000669.1:g.17284561C>A GRCh37
NC_000007.12:g.17251086C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2037C>A ENSP00000495987.1:n.-955-2037C>A
XR_927073.2:n.861+14315G>T
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