Canonical Allele Identifier: CA4172200
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs778350893
ExAC: 7:17379335 AAGT / A
gnomAD v2: 7-17379335-AAGT-A
gnomAD v3: 7-17339711-AAGT-A
gnomAD v4: 7-17339711-AAGT-A
MyVariant Identifiers: chr7:g.17379336_17379338del (hg19) chr7:g.17339713_17339715del (hg38) chr7:g.17339712_17339714del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339718_17339720del , CM000669.2:g.17339718_17339720del GRCh38
NC_000007.13:g.17379342_17379344del , CM000669.1:g.17379342_17379344del GRCh37
NC_000007.12:g.17345867_17345869del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1893_1895del MANE Select ENSP00000242057.4:p.Val632del
ENST00000637807.1:c.1863_1865del ENSP00000490530.1:p.Val622del
ENST00000642825.1:c.1848_1850del ENSP00000495987.1:p.Val617del
ENST00000242057.8:c.1893_1895del ENSP00000242057.4:p.Val632del
ENST00000463496.1:c.1893_1895del ENSP00000436466.1:p.Val632del
NM_001621.4:c.1893_1895del NP_001612.1:p.Val632del
NM_001621.5:c.1893_1895del MANE Select NP_001612.1:p.Val632del
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