Canonical Allele Identifier: CA836203352
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1300513219
gnomAD v3: 7-17298524-G-T
gnomAD v4: 7-17298524-G-T
MyVariant Identifiers: chr7:g.17338148G>T (hg19) chr7:g.17298524G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298524G>T , CM000669.2:g.17298524G>T GRCh38
NC_000007.13:g.17338148G>T , CM000669.1:g.17338148G>T GRCh37
NC_000007.12:g.17304673G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1900G>T ENSP00000495987.1:n.20+1900G>T
XR_927069.1:n.13C>A
XR_927070.1:n.13C>A
XR_927071.1:n.13C>A
XR_927072.1:n.14C>A
XR_927073.1:n.15C>A
XR_927073.2:n.15C>A
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