Canonical Allele Identifier: CA154828323
Gene: AHR HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.17298523C>T
GRCh37 chr7:g.17338147C>T
gnomAD v2:
7:17338147 C / T
gnomAD v3:
7:17298523 C / T
gnomAD v4:
chr7-17298523-C-T
Joint Max Group AF 0.39112055 (AFR)
Genomes Max Group AF 0.39216457 (AFR)
Exomes Max Group AF 0.37259655 (AFR)
dbSNP:
10249788
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298523C>T , CM000669.2:g.17298523C>T GRCh38
NC_000007.13:g.17338147C>T , CM000669.1:g.17338147C>T GRCh37
NC_000007.12:g.17304672C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.20+1899C>T ENSP00000495987.1:n.20+1899C>T
XR_927069.1:n.14G>A
XR_927070.1:n.14G>A
XR_927071.1:n.14G>A
XR_927072.1:n.15G>A
XR_927073.1:n.16G>A
XR_927073.2:n.16G>A
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