Canonical Allele Identifier: CA154824974
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs984854576
gnomAD v2: 7-17309187-T-C
gnomAD v3: 7-17269563-T-C
gnomAD v4: 7-17269563-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17269563T>C , CM000669.2:g.17269563T>C GRCh38
NC_000007.13:g.17309187T>C , CM000669.1:g.17309187T>C GRCh37
NC_000007.12:g.17275712T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.-203+21837T>C ENSP00000495987.1:n.-203+21837T>C
XR_927073.2:n.785-10235A>G