Canonical Allele Identifier: CA4172222
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs754946915
ExAC: 7:17379478 G / A
gnomAD v2: 7-17379478-G-A
gnomAD v4: 7-17339854-G-A
MyVariant Identifiers: chr7:g.17379478G>A (hg19) chr7:g.17339854G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339854G>A , CM000669.2:g.17339854G>A GRCh38
NC_000007.13:g.17379478G>A , CM000669.1:g.17379478G>A GRCh37
NC_000007.12:g.17346003G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2029G>A MANE Select ENSP00000242057.4:p.Asp677Asn
ENST00000637807.1:c.1999G>A ENSP00000490530.1:p.Asp667Asn
ENST00000642825.1:c.1984G>A ENSP00000495987.1:p.Asp662Asn
ENST00000242057.8:c.2029G>A ENSP00000242057.4:p.Asp677Asn
ENST00000463496.1:c.2029G>A ENSP00000436466.1:p.Asp677Asn
NM_001621.4:c.2029G>A NP_001612.1:p.Asp677Asn
NM_001621.5:c.2029G>A MANE Select NP_001612.1:p.Asp677Asn
Search 100 bp 5'
Search 100 bp 3'