Canonical Allele Identifier: CA454134364
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379429G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339805G>A , CM000669.2:g.17339805G>A GRCh38
NC_000007.13:g.17379429G>A , CM000669.1:g.17379429G>A GRCh37
NC_000007.12:g.17345954G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1980G>A MANE Select ENSP00000242057.4:p.Val660=
ENST00000637807.1:c.1950G>A ENSP00000490530.1:p.Val650=
ENST00000642825.1:c.1935G>A ENSP00000495987.1:p.Val645=
ENST00000242057.8:c.1980G>A ENSP00000242057.4:p.Val660=
ENST00000463496.1:c.1980G>A ENSP00000436466.1:p.Val660=
NM_001621.4:c.1980G>A NP_001612.1:p.Val660=
NM_001621.5:c.1980G>A MANE Select NP_001612.1:p.Val660=
Search 100 bp 5'
Search 100 bp 3'