Canonical Allele Identifier: CA366894460

Gene: AHR

Linked Data

• MyVariant Identifiers: chr7:g.17379022G>T (hg19) ; chr7:g.17339398G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17339398G>T , CM000669.2:g.17339398G>T	GRCh38
NC_000007.13:g.17379022G>T , CM000669.1:g.17379022G>T	GRCh37
NC_000007.12:g.17345547G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242057.9:c.1573G>T MANE Select	ENSP00000242057.4:p.Gly525Ter
ENST00000637807.1:c.1543G>T	ENSP00000490530.1:p.Gly515Ter
ENST00000642825.1:c.1528G>T	ENSP00000495987.1:p.Gly510Ter
ENST00000242057.8:c.1573G>T	ENSP00000242057.4:p.Gly525Ter
ENST00000463496.1:c.1573G>T	ENSP00000436466.1:p.Gly525Ter
ENST00000492120.1:n.555G>T
NM_001621.4:c.1573G>T	NP_001612.1:p.Gly525Ter
NM_001621.5:c.1573G>T MANE Select	NP_001612.1:p.Gly525Ter