Canonical Allele Identifier: CA2696848
Gene:

Linked Data

ClinVar Variation Id: 1338195
ClinVar RCV Id: RCV001822793
dbSNP Id: rs751991689

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765124C>G , CM000665.2:g.169765124C>G GRCh38
NC_000003.11:g.169482912C>G , CM000665.1:g.169482912C>G GRCh37
NC_000003.10:g.170965606C>G NCBI36
NG_016363.1:g.4937G>C , LRG_347:g.4937G>C