Canonical Allele Identifier: CA454134378
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379444A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339820A>C , CM000669.2:g.17339820A>C GRCh38
NC_000007.13:g.17379444A>C , CM000669.1:g.17379444A>C GRCh37
NC_000007.12:g.17345969A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1995A>C MANE Select ENSP00000242057.4:p.Pro665=
ENST00000637807.1:c.1965A>C ENSP00000490530.1:p.Pro655=
ENST00000642825.1:c.1950A>C ENSP00000495987.1:p.Pro650=
ENST00000242057.8:c.1995A>C ENSP00000242057.4:p.Pro665=
ENST00000463496.1:c.1995A>C ENSP00000436466.1:p.Pro665=
NM_001621.4:c.1995A>C NP_001612.1:p.Pro665=
NM_001621.5:c.1995A>C MANE Select NP_001612.1:p.Pro665=
Search 100 bp 5'
Search 100 bp 3'