Canonical Allele Identifier: CA154822091
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs948657871
gnomAD v3: 7-17244892-A-C
gnomAD v4: 7-17244892-A-C
MyVariant Identifiers: chr7:g.17284516A>C (hg19) chr7:g.17244892A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17244892A>C , CM000669.2:g.17244892A>C GRCh38
NC_000007.13:g.17284516A>C , CM000669.1:g.17284516A>C GRCh37
NC_000007.12:g.17251041A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-955-2082A>C ENSP00000495987.1:n.-955-2082A>C
XR_927073.2:n.861+14360T>G
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