Canonical Allele Identifier: CA2298481225
Gene:

Linked Data

dbSNP Id: rs543793905

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477652G>T , CM000680.2:g.41477652G>T GRCh38
NC_000018.9:g.39057616G>T , CM000680.1:g.39057616G>T GRCh37
NC_000018.8:g.37311614G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26482G>T