Canonical Allele Identifier: CA454134200
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379288A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339664A>C , CM000669.2:g.17339664A>C GRCh38
NC_000007.13:g.17379288A>C , CM000669.1:g.17379288A>C GRCh37
NC_000007.12:g.17345813A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1839A>C MANE Select ENSP00000242057.4:p.Val613=
ENST00000637807.1:c.1809A>C ENSP00000490530.1:p.Val603=
ENST00000642825.1:c.1794A>C ENSP00000495987.1:p.Val598=
ENST00000242057.8:c.1839A>C ENSP00000242057.4:p.Val613=
ENST00000463496.1:c.1839A>C ENSP00000436466.1:p.Val613=
NM_001621.4:c.1839A>C NP_001612.1:p.Val613=
NM_001621.5:c.1839A>C MANE Select NP_001612.1:p.Val613=
Search 100 bp 5'
Search 100 bp 3'