Canonical Allele Identifier: CA573125853
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1376889952
gnomAD v2: 7-17287171-C-G
gnomAD v3: 7-17247547-C-G
gnomAD v4: 7-17247547-C-G
MyVariant Identifiers: chr7:g.17287171C>G (hg19) chr7:g.17247547C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247547C>G , CM000669.2:g.17247547C>G GRCh38
NC_000007.13:g.17287171C>G , CM000669.1:g.17287171C>G GRCh37
NC_000007.12:g.17253696C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-382C>G ENSP00000495987.1:n.-382C>G
XR_927073.2:n.861+11705G>C
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