Canonical Allele Identifier: CA366895227
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379252G>T (hg19) chr7:g.17339628G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339628G>T , CM000669.2:g.17339628G>T GRCh38
NC_000007.13:g.17379252G>T , CM000669.1:g.17379252G>T GRCh37
NC_000007.12:g.17345777G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1803G>T MANE Select ENSP00000242057.4:p.Gln601His
ENST00000637807.1:c.1773G>T ENSP00000490530.1:p.Gln591His
ENST00000642825.1:c.1758G>T ENSP00000495987.1:p.Gln586His
ENST00000242057.8:c.1803G>T ENSP00000242057.4:p.Gln601His
ENST00000463496.1:c.1803G>T ENSP00000436466.1:p.Gln601His
NM_001621.4:c.1803G>T NP_001612.1:p.Gln601His
NM_001621.5:c.1803G>T MANE Select NP_001612.1:p.Gln601His
Search 100 bp 5'
Search 100 bp 3'