Canonical Allele Identifier: CA454134239
Gene: AHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.17379360G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17339736G>A , CM000669.2:g.17339736G>A GRCh38
NC_000007.13:g.17379360G>A , CM000669.1:g.17379360G>A GRCh37
NC_000007.12:g.17345885G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242057.9:c.1911G>A MANE Select ENSP00000242057.4:p.Gln637=
ENST00000637807.1:c.1881G>A ENSP00000490530.1:p.Gln627=
ENST00000642825.1:c.1866G>A ENSP00000495987.1:p.Gln622=
ENST00000242057.8:c.1911G>A ENSP00000242057.4:p.Gln637=
ENST00000463496.1:c.1911G>A ENSP00000436466.1:p.Gln637=
NM_001621.4:c.1911G>A NP_001612.1:p.Gln637=
NM_001621.5:c.1911G>A MANE Select NP_001612.1:p.Gln637=