Canonical Allele Identifier: CA366894918
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379118C>G (hg19) chr7:g.17339494C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339494C>G , CM000669.2:g.17339494C>G GRCh38
NC_000007.13:g.17379118C>G , CM000669.1:g.17379118C>G GRCh37
NC_000007.12:g.17345643C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000242057.9:c.1669C>G MANE Select ENSP00000242057.4:p.Gln557Glu
ENST00000637807.1:c.1639C>G ENSP00000490530.1:p.Gln547Glu
ENST00000642825.1:c.1624C>G ENSP00000495987.1:p.Gln542Glu
ENST00000242057.8:c.1669C>G ENSP00000242057.4:p.Gln557Glu
ENST00000463496.1:c.1669C>G ENSP00000436466.1:p.Gln557Glu
ENST00000492120.1:n.651C>G
NM_001621.4:c.1669C>G NP_001612.1:p.Gln557Glu
NM_001621.5:c.1669C>G MANE Select NP_001612.1:p.Gln557Glu
Search 100 bp 5'
Search 100 bp 3'