Canonical Allele Identifier: CA154826862
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1011422268
MyVariant Identifiers: chr7:g.17325154A>C (hg19) chr7:g.17285530A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285530A>C , CM000669.2:g.17285530A>C GRCh38
NC_000007.13:g.17325154A>C , CM000669.1:g.17325154A>C GRCh37
NC_000007.12:g.17291679A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10767A>C ENSP00000495987.1:n.-202-10767A>C
XR_927069.1:n.567+713T>G
XR_927070.1:n.567+713T>G
XR_927071.1:n.567+713T>G
XR_927072.1:n.568+713T>G
XR_927073.2:n.711+713T>G
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