Canonical Allele Identifier: CA454049399
Gene: AHR HGNC NCBI

Linked Data

dbSNP Id: rs41351350
MyVariant Identifiers: chr7:g.17338055G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17298431G>C , CM000669.2:g.17298431G>C GRCh38
NC_000007.13:g.17338055G>C , CM000669.1:g.17338055G>C GRCh37
NC_000007.12:g.17304580G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000642825.1:c.20+1807G>C ENSP00000495987.1:n.20+1807G>C
XR_927069.1:n.106C>G
XR_927070.1:n.106C>G
XR_927071.1:n.106C>G
XR_927072.1:n.107C>G
XR_927073.1:n.108C>G
XR_927073.2:n.108C>G