Canonical Allele Identifier: CA454045303

Gene: AHR

Linked Data

• dbSNP Id: rs1781753315
• MyVariant Identifiers: chr7:g.17325145A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17285521A>G , CM000669.2:g.17285521A>G	GRCh38
NC_000007.13:g.17325145A>G , CM000669.1:g.17325145A>G	GRCh37
NC_000007.12:g.17291670A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-10776A>G	ENSP00000495987.1:n.-202-10776A>G
XR_927069.1:n.567+722T>C
XR_927070.1:n.567+722T>C
XR_927071.1:n.567+722T>C
XR_927072.1:n.568+722T>C
XR_927073.2:n.711+722T>C