Canonical Allele Identifier: CA573130673
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs1429121335
gnomAD v2: 7-17325019-T-C
gnomAD v3: 7-17285395-T-C
gnomAD v4: 7-17285395-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285395T>C , CM000669.2:g.17285395T>C GRCh38
NC_000007.13:g.17325019T>C , CM000669.1:g.17325019T>C GRCh37
NC_000007.12:g.17291544T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10902T>C ENSP00000495987.1:n.-202-10902T>C
XR_927069.1:n.567+848A>G
XR_927070.1:n.567+848A>G
XR_927071.1:n.567+848A>G
XR_927072.1:n.568+848A>G
XR_927073.2:n.711+848A>G