Canonical Allele Identifier: CA454049409
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17298432-C-T
MyVariant Identifiers: chr7:g.17338056C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298432C>T , CM000669.2:g.17298432C>T GRCh38
NC_000007.13:g.17338056C>T , CM000669.1:g.17338056C>T GRCh37
NC_000007.12:g.17304581C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1808C>T ENSP00000495987.1:n.20+1808C>T
XR_927069.1:n.105G>A
XR_927070.1:n.105G>A
XR_927071.1:n.105G>A
XR_927072.1:n.106G>A
XR_927073.1:n.107G>A
XR_927073.2:n.107G>A
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