Canonical Allele Identifier: CA366894438
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379017T>C (hg19) chr7:g.17339393T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339393T>C , CM000669.2:g.17339393T>C GRCh38
NC_000007.13:g.17379017T>C , CM000669.1:g.17379017T>C GRCh37
NC_000007.12:g.17345542T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1568T>C MANE Select ENSP00000242057.4:p.Phe523Ser
ENST00000637807.1:c.1538T>C ENSP00000490530.1:p.Phe513Ser
ENST00000642825.1:c.1523T>C ENSP00000495987.1:p.Phe508Ser
ENST00000242057.8:c.1568T>C ENSP00000242057.4:p.Phe523Ser
ENST00000463496.1:c.1568T>C ENSP00000436466.1:p.Phe523Ser
ENST00000492120.1:n.550T>C
NM_001621.4:c.1568T>C NP_001612.1:p.Phe523Ser
NM_001621.5:c.1568T>C MANE Select NP_001612.1:p.Phe523Ser
Search 100 bp 5'
Search 100 bp 3'