Canonical Allele Identifier: CA573128445
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1158991062
gnomAD v2: 7-17309196-C-T
gnomAD v3: 7-17269572-C-T
gnomAD v4: 7-17269572-C-T
MyVariant Identifiers: chr7:g.17309196C>T (hg19) chr7:g.17269572C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269572C>T , CM000669.2:g.17269572C>T GRCh38
NC_000007.13:g.17309196C>T , CM000669.1:g.17309196C>T GRCh37
NC_000007.12:g.17275721C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-203+21846C>T ENSP00000495987.1:n.-203+21846C>T
XR_927073.2:n.785-10244G>A
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