Canonical Allele Identifier: CA2681907555
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17247554-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17247554T>C , CM000669.2:g.17247554T>C GRCh38
NC_000007.13:g.17287178T>C , CM000669.1:g.17287178T>C GRCh37
NC_000007.12:g.17253703T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-375T>C ENSP00000495987.1:n.-375T>C
XR_927073.2:n.861+11698A>G
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