Canonical Allele Identifier: CA723156272
Gene:

Linked Data

ClinVar Variation Id: 2681855
ClinVar RCV Id: RCV003477147
dbSNP Id: rs1194528351

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737122A>G , CM000678.2:g.68737122A>G GRCh38
NC_000016.9:g.68771025A>G , CM000678.1:g.68771025A>G GRCh37
NC_000016.8:g.67328526A>G NCBI36
NG_008021.1:g.4831A>G , LRG_301:g.4831A>G