Canonical Allele Identifier: CA836218831
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1290840495
MyVariant Identifiers: chr7:g.17284553A>C (hg19) chr7:g.17244929A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244929A>C , CM000669.2:g.17244929A>C GRCh38
NC_000007.13:g.17284553A>C , CM000669.1:g.17284553A>C GRCh37
NC_000007.12:g.17251078A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2045A>C ENSP00000495987.1:n.-955-2045A>C
XR_927073.2:n.861+14323T>G
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