Canonical Allele Identifier: CA2681909912
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339604-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339606del , CM000669.2:g.17339606del GRCh38
NC_000007.13:g.17379230del , CM000669.1:g.17379230del GRCh37
NC_000007.12:g.17345755del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1781del MANE Select ENSP00000242057.4:p.Phe594SerfsTer14
ENST00000637807.1:c.1751del ENSP00000490530.1:p.Phe584SerfsTer14
ENST00000642825.1:c.1736del ENSP00000495987.1:p.Phe579SerfsTer14
ENST00000242057.8:c.1781del ENSP00000242057.4:p.Phe594SerfsTer14
ENST00000463496.1:c.1781del ENSP00000436466.1:p.Phe594SerfsTer14
NM_001621.4:c.1781del NP_001612.1:p.Phe594SerfsTer14
NM_001621.5:c.1781del MANE Select NP_001612.1:p.Phe594SerfsTer14
Search 100 bp 5'
Search 100 bp 3'