Canonical Allele Identifier: CA836200023
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1453633969
gnomAD v3: 7-17293313-G-T
gnomAD v4: 7-17293313-G-T
MyVariant Identifiers: chr7:g.17332937G>T (hg19) chr7:g.17293313G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293313G>T , CM000669.2:g.17293313G>T GRCh38
NC_000007.13:g.17332937G>T , CM000669.1:g.17332937G>T GRCh37
NC_000007.12:g.17299462G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2984G>T ENSP00000495987.1:n.-202-2984G>T
XR_927069.1:n.293+1853C>A
XR_927070.1:n.293+1853C>A
XR_927071.1:n.293+1853C>A
XR_927072.1:n.294+1853C>A
XR_927073.1:n.295+1853C>A
XR_927073.2:n.295+1853C>A
Search 100 bp 5'
Search 100 bp 3'