Canonical Allele Identifier: CA836218848
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1359351701
gnomAD v3: 7-17244932-G-T
gnomAD v4: 7-17244932-G-T
MyVariant Identifiers: chr7:g.17284556G>T (hg19) chr7:g.17244932G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244932G>T , CM000669.2:g.17244932G>T GRCh38
NC_000007.13:g.17284556G>T , CM000669.1:g.17284556G>T GRCh37
NC_000007.12:g.17251081G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2042G>T ENSP00000495987.1:n.-955-2042G>T
XR_927073.2:n.861+14320C>A
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