Canonical Allele Identifier: CA309961769
Gene:

Linked Data

dbSNP Id: rs1055350416
MyVariant Identifiers: chr19:g.54871528G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54871528G>T , CM000681.2:g.54871528G>T GRCh38
NC_000019.8:g.60074796G>T NCBI36