Canonical Allele Identifier: CA106421619
Gene:

Linked Data

dbSNP Id: rs1027180154

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601547T>G , CM000666.2:g.134601547T>G GRCh38
NC_000004.11:g.135522702T>G , CM000666.1:g.135522702T>G GRCh37
NC_000004.10:g.135742152T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14188T>G
XR_939214.1:n.392+14188T>G
XR_939214.2:n.392+14188T>G