Canonical Allele Identifier: CA454134185
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1584043491
MyVariant Identifiers: chr7:g.17379261C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339637C>T , CM000669.2:g.17339637C>T GRCh38
NC_000007.13:g.17379261C>T , CM000669.1:g.17379261C>T GRCh37
NC_000007.12:g.17345786C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1812C>T MANE Select ENSP00000242057.4:p.Ser604=
ENST00000637807.1:c.1782C>T ENSP00000490530.1:p.Ser594=
ENST00000642825.1:c.1767C>T ENSP00000495987.1:p.Ser589=
ENST00000242057.8:c.1812C>T ENSP00000242057.4:p.Ser604=
ENST00000463496.1:c.1812C>T ENSP00000436466.1:p.Ser604=
NM_001621.4:c.1812C>T NP_001612.1:p.Ser604=
NM_001621.5:c.1812C>T MANE Select NP_001612.1:p.Ser604=
Search 100 bp 5'
Search 100 bp 3'