Canonical Allele Identifier: CA366894924

Gene: AHR

Linked Data

• MyVariant Identifiers: chr7:g.17379120G>T (hg19) ; chr7:g.17339496G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339496G>T , CM000669.2:g.17339496G>T	GRCh38
NC_000007.13:g.17379120G>T , CM000669.1:g.17379120G>T	GRCh37
NC_000007.12:g.17345645G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000242057.9:c.1671G>T MANE Select	ENSP00000242057.4:p.Gln557His
ENST00000637807.1:c.1641G>T	ENSP00000490530.1:p.Gln547His
ENST00000642825.1:c.1626G>T	ENSP00000495987.1:p.Gln542His
ENST00000242057.8:c.1671G>T	ENSP00000242057.4:p.Gln557His
ENST00000463496.1:c.1671G>T	ENSP00000436466.1:p.Gln557His
ENST00000492120.1:n.653G>T
NM_001621.4:c.1671G>T	NP_001612.1:p.Gln557His
NM_001621.5:c.1671G>T MANE Select	NP_001612.1:p.Gln557His