Canonical Allele Identifier: CA454049366

Gene: AHR

Linked Data

• MyVariant Identifiers: chr7:g.17338049A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17298425A>G , CM000669.2:g.17298425A>G	GRCh38
NC_000007.13:g.17338049A>G , CM000669.1:g.17338049A>G	GRCh37
NC_000007.12:g.17304574A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.20+1801A>G	ENSP00000495987.1:n.20+1801A>G
XR_927069.1:n.112T>C
XR_927070.1:n.112T>C
XR_927071.1:n.112T>C
XR_927072.1:n.113T>C
XR_927073.1:n.114T>C
XR_927073.2:n.114T>C