Canonical Allele Identifier: CA366895682
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379446A>T (hg19) chr7:g.17339822A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339822A>T , CM000669.2:g.17339822A>T GRCh38
NC_000007.13:g.17379446A>T , CM000669.1:g.17379446A>T GRCh37
NC_000007.12:g.17345971A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1997A>T MANE Select ENSP00000242057.4:p.Gln666Leu
ENST00000637807.1:c.1967A>T ENSP00000490530.1:p.Gln656Leu
ENST00000642825.1:c.1952A>T ENSP00000495987.1:p.Gln651Leu
ENST00000242057.8:c.1997A>T ENSP00000242057.4:p.Gln666Leu
ENST00000463496.1:c.1997A>T ENSP00000436466.1:p.Gln666Leu
NM_001621.4:c.1997A>T NP_001612.1:p.Gln666Leu
NM_001621.5:c.1997A>T MANE Select NP_001612.1:p.Gln666Leu
Search 100 bp 5'
Search 100 bp 3'