Canonical Allele Identifier: CA915432518
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1562467887
gnomAD v2: 7-17325117-T-A
gnomAD v3: 7-17285493-T-A
gnomAD v4: 7-17285493-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285493T>A , CM000669.2:g.17285493T>A GRCh38
NC_000007.13:g.17325117T>A , CM000669.1:g.17325117T>A GRCh37
NC_000007.12:g.17291642T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10804T>A ENSP00000495987.1:n.-202-10804T>A
XR_927069.1:n.567+750A>T
XR_927070.1:n.567+750A>T
XR_927071.1:n.567+750A>T
XR_927072.1:n.568+750A>T
XR_927073.2:n.711+750A>T
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