Canonical Allele Identifier: CA154826850

Gene: AHR

Linked Data

• dbSNP Id: rs561353562
• MyVariant Identifiers: chr7:g.17325084C>T (hg19) ; chr7:g.17285460C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285460C>T , CM000669.2:g.17285460C>T	GRCh38
NC_000007.13:g.17325084C>T , CM000669.1:g.17325084C>T	GRCh37
NC_000007.12:g.17291609C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-10837C>T	ENSP00000495987.1:n.-202-10837C>T
XR_927069.1:n.567+783G>A
XR_927070.1:n.567+783G>A
XR_927071.1:n.567+783G>A
XR_927072.1:n.568+783G>A
XR_927073.2:n.711+783G>A