Canonical Allele Identifier: CA12582207
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs41351350
gnomAD v2: 7-17338055-G-A
gnomAD v3: 7-17298431-G-A
gnomAD v4: 7-17298431-G-A
MyVariant Identifiers: chr7:g.17338055G>A (hg19) chr7:g.17298431G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298431G>A , CM000669.2:g.17298431G>A GRCh38
NC_000007.13:g.17338055G>A , CM000669.1:g.17338055G>A GRCh37
NC_000007.12:g.17304580G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.20+1807G>A ENSP00000495987.1:n.20+1807G>A
XR_927069.1:n.106C>T
XR_927070.1:n.106C>T
XR_927071.1:n.106C>T
XR_927072.1:n.107C>T
XR_927073.1:n.108C>T
XR_927073.2:n.108C>T
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