Canonical Allele Identifier: CA154827728
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs770822111
MyVariant Identifiers: chr7:g.17332863T>G (hg19) chr7:g.17293239T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293239T>G , CM000669.2:g.17293239T>G GRCh38
NC_000007.13:g.17332863T>G , CM000669.1:g.17332863T>G GRCh37
NC_000007.12:g.17299388T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-202-3058T>G ENSP00000495987.1:n.-202-3058T>G
XR_927069.1:n.293+1927A>C
XR_927070.1:n.293+1927A>C
XR_927071.1:n.293+1927A>C
XR_927072.1:n.294+1927A>C
XR_927073.1:n.296-1868A>C
XR_927073.2:n.296-1868A>C
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