Canonical Allele Identifier: CA573132031

Gene: AHR

Linked Data

• dbSNP Id: rs1351413876
• gnomAD v2: 7-17332927-T-C
• gnomAD v3: 7-17293303-T-C
• gnomAD v4: 7-17293303-T-C
• MyVariant Identifiers: chr7:g.17332927T>C (hg19) ; chr7:g.17293303T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17293303T>C , CM000669.2:g.17293303T>C	GRCh38
NC_000007.13:g.17332927T>C , CM000669.1:g.17332927T>C	GRCh37
NC_000007.12:g.17299452T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000642825.1:c.-202-2994T>C	ENSP00000495987.1:n.-202-2994T>C
XR_927069.1:n.293+1863A>G
XR_927070.1:n.293+1863A>G
XR_927071.1:n.293+1863A>G
XR_927072.1:n.294+1863A>G
XR_927073.1:n.295+1863A>G
XR_927073.2:n.295+1863A>G