Canonical Allele Identifier: CA154827763

Gene: AHR

Linked Data

• dbSNP Id: rs941494692
• gnomAD v2: 7-17333143-T-C
• gnomAD v3: 7-17293519-T-C
• gnomAD v4: 7-17293519-T-C
• MyVariant Identifiers: chr7:g.17333143T>C (hg19) ; chr7:g.17293519T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293519T>C , CM000669.2:g.17293519T>C	GRCh38
NC_000007.13:g.17333143T>C , CM000669.1:g.17333143T>C	GRCh37
NC_000007.12:g.17299668T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642825.1:c.-202-2778T>C	ENSP00000495987.1:n.-202-2778T>C
XR_927069.1:n.293+1647A>G
XR_927070.1:n.293+1647A>G
XR_927071.1:n.293+1647A>G
XR_927072.1:n.294+1647A>G
XR_927073.1:n.295+1647A>G
XR_927073.2:n.295+1647A>G