Canonical Allele Identifier: CA366895614
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1522776
ClinVar RCV Id: RCV002036255
dbSNP Id: rs1199321600
gnomAD v2: 7-17379416-C-G
gnomAD v4: 7-17339792-C-G
MyVariant Identifiers: chr7:g.17379416C>G (hg19) chr7:g.17339792C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339792C>G , CM000669.2:g.17339792C>G GRCh38
NC_000007.13:g.17379416C>G , CM000669.1:g.17379416C>G GRCh37
NC_000007.12:g.17345941C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1967C>G MANE Select ENSP00000242057.4:p.Ser656Cys
ENST00000637807.1:c.1937C>G ENSP00000490530.1:p.Ser646Cys
ENST00000642825.1:c.1922C>G ENSP00000495987.1:p.Ser641Cys
ENST00000242057.8:c.1967C>G ENSP00000242057.4:p.Ser656Cys
ENST00000463496.1:c.1967C>G ENSP00000436466.1:p.Ser656Cys
NM_001621.4:c.1967C>G NP_001612.1:p.Ser656Cys
NM_001621.5:c.1967C>G MANE Select NP_001612.1:p.Ser656Cys
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