Canonical Allele Identifier: CA366895426
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 964083
ClinVar RCV Id: RCV001238230
dbSNP Id: rs1782398060
gnomAD v4: 7-17339714-T-C
MyVariant Identifiers: chr7:g.17379338T>C (hg19) chr7:g.17339714T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339714T>C , CM000669.2:g.17339714T>C GRCh38
NC_000007.13:g.17379338T>C , CM000669.1:g.17379338T>C GRCh37
NC_000007.12:g.17345863T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1889T>C MANE Select ENSP00000242057.4:p.Val630Ala
ENST00000637807.1:c.1859T>C ENSP00000490530.1:p.Val620Ala
ENST00000642825.1:c.1844T>C ENSP00000495987.1:p.Val615Ala
ENST00000242057.8:c.1889T>C ENSP00000242057.4:p.Val630Ala
ENST00000463496.1:c.1889T>C ENSP00000436466.1:p.Val630Ala
NM_001621.4:c.1889T>C NP_001612.1:p.Val630Ala
NM_001621.5:c.1889T>C MANE Select NP_001612.1:p.Val630Ala
Search 100 bp 5'
Search 100 bp 3'