Canonical Allele Identifier: CA573128442
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1185381098
gnomAD v2: 7-17309179-C-T
gnomAD v3: 7-17269555-C-T
gnomAD v4: 7-17269555-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269555C>T , CM000669.2:g.17269555C>T GRCh38
NC_000007.13:g.17309179C>T , CM000669.1:g.17309179C>T GRCh37
NC_000007.12:g.17275704C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21829C>T ENSP00000495987.1:n.-203+21829C>T
XR_927073.2:n.785-10227G>A