Canonical Allele Identifier: CA311095646
Gene:

Linked Data

dbSNP Id: rs1025051368
MyVariant Identifiers: chr20:g.4717986C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4717986C>T , CM000682.2:g.4717986C>T GRCh38
NC_000020.10:g.4698632C>T , CM000682.1:g.4698632C>T GRCh37
NC_000020.9:g.4646632C>T NCBI36