Canonical Allele Identifier: CA4172203
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1579996
ClinVar RCV Id: RCV002094702
dbSNP Id: rs765822318
ExAC: 7:17379363 G / C
gnomAD v2: 7-17379363-G-C
gnomAD v3: 7-17339739-G-C
gnomAD v4: 7-17339739-G-C
MyVariant Identifiers: chr7:g.17379363G>C (hg19) chr7:g.17339739G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339739G>C , CM000669.2:g.17339739G>C GRCh38
NC_000007.13:g.17379363G>C , CM000669.1:g.17379363G>C GRCh37
NC_000007.12:g.17345888G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1914G>C MANE Select ENSP00000242057.4:p.Leu638=
ENST00000637807.1:c.1884G>C ENSP00000490530.1:p.Leu628=
ENST00000642825.1:c.1869G>C ENSP00000495987.1:p.Leu623=
ENST00000242057.8:c.1914G>C ENSP00000242057.4:p.Leu638=
ENST00000463496.1:c.1914G>C ENSP00000436466.1:p.Leu638=
NM_001621.4:c.1914G>C NP_001612.1:p.Leu638=
NM_001621.5:c.1914G>C MANE Select NP_001612.1:p.Leu638=
Search 100 bp 5'
Search 100 bp 3'