Canonical Allele Identifier: CA454134116
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379123T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339499T>C , CM000669.2:g.17339499T>C GRCh38
NC_000007.13:g.17379123T>C , CM000669.1:g.17379123T>C GRCh37
NC_000007.12:g.17345648T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000242057.9:c.1674T>C MANE Select ENSP00000242057.4:p.Asn558=
ENST00000637807.1:c.1644T>C ENSP00000490530.1:p.Asn548=
ENST00000642825.1:c.1629T>C ENSP00000495987.1:p.Asn543=
ENST00000242057.8:c.1674T>C ENSP00000242057.4:p.Asn558=
ENST00000463496.1:c.1674T>C ENSP00000436466.1:p.Asn558=
ENST00000492120.1:n.656T>C
NM_001621.4:c.1674T>C NP_001612.1:p.Asn558=
NM_001621.5:c.1674T>C MANE Select NP_001612.1:p.Asn558=
Search 100 bp 5'
Search 100 bp 3'