Canonical Allele Identifier: CA154827739

Gene: AHR

Linked Data

• dbSNP Id: rs569500006
• gnomAD v2: 7-17332923-A-T
• gnomAD v3: 7-17293299-A-T
• gnomAD v4: 7-17293299-A-T
• MyVariant Identifiers: chr7:g.17332923A>T (hg19) ; chr7:g.17293299A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293299A>T , CM000669.2:g.17293299A>T	GRCh38
NC_000007.13:g.17332923A>T , CM000669.1:g.17332923A>T	GRCh37
NC_000007.12:g.17299448A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-2998A>T	ENSP00000495987.1:n.-202-2998A>T
XR_927069.1:n.293+1867T>A
XR_927070.1:n.293+1867T>A
XR_927071.1:n.293+1867T>A
XR_927072.1:n.294+1867T>A
XR_927073.1:n.295+1867T>A
XR_927073.2:n.295+1867T>A