Canonical Allele Identifier: CA454134235
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1651586
ClinVar RCV Id: RCV002151906
dbSNP Id: rs1370705419
gnomAD v2: 7-17379351-A-G
gnomAD v3: 7-17339727-A-G
gnomAD v4: 7-17339727-A-G
MyVariant Identifiers: chr7:g.17379351A>G (hg19) chr7:g.17339727A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339727A>G , CM000669.2:g.17339727A>G GRCh38
NC_000007.13:g.17379351A>G , CM000669.1:g.17379351A>G GRCh37
NC_000007.12:g.17345876A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1902A>G MANE Select ENSP00000242057.4:p.Pro634=
ENST00000637807.1:c.1872A>G ENSP00000490530.1:p.Pro624=
ENST00000642825.1:c.1857A>G ENSP00000495987.1:p.Pro619=
ENST00000242057.8:c.1902A>G ENSP00000242057.4:p.Pro634=
ENST00000463496.1:c.1902A>G ENSP00000436466.1:p.Pro634=
NM_001621.4:c.1902A>G NP_001612.1:p.Pro634=
NM_001621.5:c.1902A>G MANE Select NP_001612.1:p.Pro634=
Search 100 bp 5'
Search 100 bp 3'