Canonical Allele Identifier: CA154827748
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs763333984
gnomAD v2: 7-17333007-T-C
gnomAD v3: 7-17293383-T-C
gnomAD v4: 7-17293383-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17293383T>C , CM000669.2:g.17293383T>C GRCh38
NC_000007.13:g.17333007T>C , CM000669.1:g.17333007T>C GRCh37
NC_000007.12:g.17299532T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000642825.1:c.-202-2914T>C ENSP00000495987.1:n.-202-2914T>C
XR_927069.1:n.293+1783A>G
XR_927070.1:n.293+1783A>G
XR_927071.1:n.293+1783A>G
XR_927072.1:n.294+1783A>G
XR_927073.1:n.295+1783A>G
XR_927073.2:n.295+1783A>G