Canonical Allele Identifier: CA1098896355
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1781835677
gnomAD v3: 7-17293221-C-T
gnomAD v4: 7-17293221-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293221C>T , CM000669.2:g.17293221C>T GRCh38
NC_000007.13:g.17332845C>T , CM000669.1:g.17332845C>T GRCh37
NC_000007.12:g.17299370C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-3076C>T ENSP00000495987.1:n.-202-3076C>T
XR_927069.1:n.293+1945G>A
XR_927070.1:n.293+1945G>A
XR_927071.1:n.293+1945G>A
XR_927072.1:n.294+1945G>A
XR_927073.1:n.296-1850G>A
XR_927073.2:n.296-1850G>A
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