Canonical Allele Identifier: CA4172205
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1908283
ClinVar RCV Id: RCV002581443
dbSNP Id: rs754999844
ExAC: 7:17379372 G / A
gnomAD v2: 7-17379372-G-A
gnomAD v3: 7-17339748-G-A
gnomAD v4: 7-17339748-G-A
MyVariant Identifiers: chr7:g.17379372G>A (hg19) chr7:g.17339748G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339748G>A , CM000669.2:g.17339748G>A GRCh38
NC_000007.13:g.17379372G>A , CM000669.1:g.17379372G>A GRCh37
NC_000007.12:g.17345897G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1923G>A MANE Select ENSP00000242057.4:p.Lys641=
ENST00000637807.1:c.1893G>A ENSP00000490530.1:p.Lys631=
ENST00000642825.1:c.1878G>A ENSP00000495987.1:p.Lys626=
ENST00000242057.8:c.1923G>A ENSP00000242057.4:p.Lys641=
ENST00000463496.1:c.1923G>A ENSP00000436466.1:p.Lys641=
NM_001621.4:c.1923G>A NP_001612.1:p.Lys641=
NM_001621.5:c.1923G>A MANE Select NP_001612.1:p.Lys641=
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