Canonical Allele Identifier: CA366895755
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1782399782
MyVariant Identifiers: chr7:g.17379476C>G (hg19) chr7:g.17339852C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339852C>G , CM000669.2:g.17339852C>G GRCh38
NC_000007.13:g.17379476C>G , CM000669.1:g.17379476C>G GRCh37
NC_000007.12:g.17346001C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2027C>G MANE Select ENSP00000242057.4:p.Thr676Arg
ENST00000637807.1:c.1997C>G ENSP00000490530.1:p.Thr666Arg
ENST00000642825.1:c.1982C>G ENSP00000495987.1:p.Thr661Arg
ENST00000242057.8:c.2027C>G ENSP00000242057.4:p.Thr676Arg
ENST00000463496.1:c.2027C>G ENSP00000436466.1:p.Thr676Arg
NM_001621.4:c.2027C>G NP_001612.1:p.Thr676Arg
NM_001621.5:c.2027C>G MANE Select NP_001612.1:p.Thr676Arg
Search 100 bp 5'
Search 100 bp 3'