Canonical Allele Identifier: CA15689274
Gene:

Linked Data

ClinVar Variation Id: 1277343
ClinVar RCV Id: RCV001692500
dbSNP Id: rs12718463

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116835627T>C , CM000673.2:g.116835627T>C GRCh38
NC_000011.9:g.116706343T>C , CM000673.1:g.116706343T>C GRCh37
NC_000011.8:g.116211553T>C NCBI36
NG_012021.1:g.6996A>G , LRG_767:g.6996A>G