Canonical Allele Identifier: CA4172219
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs760250596
ExAC: 7:17379465 T / C
gnomAD v2: 7-17379465-T-C
gnomAD v3: 7-17339841-T-C
gnomAD v4: 7-17339841-T-C
MyVariant Identifiers: chr7:g.17379465T>C (hg19) chr7:g.17339841T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339841T>C , CM000669.2:g.17339841T>C GRCh38
NC_000007.13:g.17379465T>C , CM000669.1:g.17379465T>C GRCh37
NC_000007.12:g.17345990T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2016T>C MANE Select ENSP00000242057.4:p.Tyr672=
ENST00000637807.1:c.1986T>C ENSP00000490530.1:p.Tyr662=
ENST00000642825.1:c.1971T>C ENSP00000495987.1:p.Tyr657=
ENST00000242057.8:c.2016T>C ENSP00000242057.4:p.Tyr672=
ENST00000463496.1:c.2016T>C ENSP00000436466.1:p.Tyr672=
NM_001621.4:c.2016T>C NP_001612.1:p.Tyr672=
NM_001621.5:c.2016T>C MANE Select NP_001612.1:p.Tyr672=
Search 100 bp 5'
Search 100 bp 3'