Canonical Allele Identifier: CA1691255509
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1584003465
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244878A>C , CM000669.2:g.17244878A>C GRCh38
NC_000007.13:g.17284502A>C , CM000669.1:g.17284502A>C GRCh37
NC_000007.12:g.17251027A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2096A>C ENSP00000495987.1:n.-955-2096A>C
XR_927073.2:n.861+14374T>G
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