Canonical Allele Identifier: CA154826868
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs965658859
gnomAD v3: 7-17285569-A-C
gnomAD v4: 7-17285569-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17285569A>C , CM000669.2:g.17285569A>C GRCh38
NC_000007.13:g.17325193A>C , CM000669.1:g.17325193A>C GRCh37
NC_000007.12:g.17291718A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-10728A>C ENSP00000495987.1:n.-202-10728A>C
XR_927069.1:n.567+674T>G
XR_927070.1:n.567+674T>G
XR_927071.1:n.567+674T>G
XR_927072.1:n.568+674T>G
XR_927073.2:n.711+674T>G