Canonical Allele Identifier: CA154826869
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs976120307
gnomAD v3: 7-17285572-T-C
gnomAD v4: 7-17285572-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285572T>C , CM000669.2:g.17285572T>C GRCh38
NC_000007.13:g.17325196T>C , CM000669.1:g.17325196T>C GRCh37
NC_000007.12:g.17291721T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10725T>C ENSP00000495987.1:n.-202-10725T>C
XR_927069.1:n.567+671A>G
XR_927070.1:n.567+671A>G
XR_927071.1:n.567+671A>G
XR_927072.1:n.568+671A>G
XR_927073.2:n.711+671A>G