Canonical Allele Identifier: CA454134178
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs371295244
gnomAD v3: 7-17339616-A-C
gnomAD v4: 7-17339616-A-C
MyVariant Identifiers: chr7:g.17379240A>C (hg19) chr7:g.17339616A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339616A>C , CM000669.2:g.17339616A>C GRCh38
NC_000007.13:g.17379240A>C , CM000669.1:g.17379240A>C GRCh37
NC_000007.12:g.17345765A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1791A>C MANE Select ENSP00000242057.4:p.Ser597=
ENST00000637807.1:c.1761A>C ENSP00000490530.1:p.Ser587=
ENST00000642825.1:c.1746A>C ENSP00000495987.1:p.Ser582=
ENST00000242057.8:c.1791A>C ENSP00000242057.4:p.Ser597=
ENST00000463496.1:c.1791A>C ENSP00000436466.1:p.Ser597=
NM_001621.4:c.1791A>C NP_001612.1:p.Ser597=
NM_001621.5:c.1791A>C MANE Select NP_001612.1:p.Ser597=
Search 100 bp 5'
Search 100 bp 3'