Canonical Allele Identifier: CA366895730
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379465T>G (hg19) chr7:g.17339841T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339841T>G , CM000669.2:g.17339841T>G GRCh38
NC_000007.13:g.17379465T>G , CM000669.1:g.17379465T>G GRCh37
NC_000007.12:g.17345990T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.2016T>G MANE Select ENSP00000242057.4:p.Tyr672Ter
ENST00000637807.1:c.1986T>G ENSP00000490530.1:p.Tyr662Ter
ENST00000642825.1:c.1971T>G ENSP00000495987.1:p.Tyr657Ter
ENST00000242057.8:c.2016T>G ENSP00000242057.4:p.Tyr672Ter
ENST00000463496.1:c.2016T>G ENSP00000436466.1:p.Tyr672Ter
NM_001621.4:c.2016T>G NP_001612.1:p.Tyr672Ter
NM_001621.5:c.2016T>G MANE Select NP_001612.1:p.Tyr672Ter
Search 100 bp 5'
Search 100 bp 3'