Canonical Allele Identifier: CA50663554
Gene:

Linked Data

dbSNP Id: rs1016446462
MyVariant Identifiers: chr2:g.76148303G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.76148303G>T , CM000664.2:g.76148303G>T GRCh38
NC_000002.11:g.76375429G>T , CM000664.1:g.76375429G>T GRCh37
NC_000002.10:g.76228937G>T NCBI36