Canonical Allele Identifier: CA4172223
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs138094242
ExAC: 7:17379479 A / T
gnomAD v2: 7-17379479-A-T
MyVariant Identifiers: chr7:g.17379479A>T (hg19) chr7:g.17339855A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339855A>T , CM000669.2:g.17339855A>T GRCh38
NC_000007.13:g.17379479A>T , CM000669.1:g.17379479A>T GRCh37
NC_000007.12:g.17346004A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2030A>T MANE Select ENSP00000242057.4:p.Asp677Val
ENST00000637807.1:c.2000A>T ENSP00000490530.1:p.Asp667Val
ENST00000642825.1:c.1985A>T ENSP00000495987.1:p.Asp662Val
ENST00000242057.8:c.2030A>T ENSP00000242057.4:p.Asp677Val
ENST00000463496.1:c.2030A>T ENSP00000436466.1:p.Asp677Val
NM_001621.4:c.2030A>T NP_001612.1:p.Asp677Val
NM_001621.5:c.2030A>T MANE Select NP_001612.1:p.Asp677Val
Search 100 bp 5'
Search 100 bp 3'