Canonical Allele Identifier: CA229293685
Gene:

Linked Data

dbSNP Id: rs956146628
MyVariant Identifiers: chr11:g.116748156C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116748156C>T , CM000673.2:g.116748156C>T GRCh38
NC_000011.9:g.116618872C>T , CM000673.1:g.116618872C>T GRCh37
NC_000011.8:g.116124082C>T NCBI36