Canonical Allele Identifier: CA366895762
Gene: AHR HGNC NCBI

Linked Data

gnomAD v4: 7-17339856-C-G
MyVariant Identifiers: chr7:g.17379480C>G (hg19) chr7:g.17339856C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339856C>G , CM000669.2:g.17339856C>G GRCh38
NC_000007.13:g.17379480C>G , CM000669.1:g.17379480C>G GRCh37
NC_000007.12:g.17346005C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2031C>G MANE Select ENSP00000242057.4:p.Asp677Glu
ENST00000637807.1:c.2001C>G ENSP00000490530.1:p.Asp667Glu
ENST00000642825.1:c.1986C>G ENSP00000495987.1:p.Asp662Glu
ENST00000242057.8:c.2031C>G ENSP00000242057.4:p.Asp677Glu
ENST00000463496.1:c.2031C>G ENSP00000436466.1:p.Asp677Glu
NM_001621.4:c.2031C>G NP_001612.1:p.Asp677Glu
NM_001621.5:c.2031C>G MANE Select NP_001612.1:p.Asp677Glu
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