Canonical Allele Identifier: CA212166522
Gene:

Linked Data

dbSNP Id: rs912301286
MyVariant Identifiers: chr10:g.101750691C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750691C>A , CM000672.2:g.101750691C>A GRCh38
NC_000010.10:g.103510448C>A , CM000672.1:g.103510448C>A GRCh37
NC_000010.9:g.103500438C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946255.1:n.217-6474G>T
XR_946255.2:n.217-6474G>T