Canonical Allele Identifier: CA64810677
Gene:

Linked Data

ClinVar Variation Id: 1287291
ClinVar RCV Id: RCV001708916
dbSNP Id: rs13022992

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214809712C>T , CM000664.2:g.214809712C>T GRCh38
NC_000002.11:g.215674436C>T , CM000664.1:g.215674436C>T GRCh37
NC_000002.10:g.215382681C>T NCBI36
NG_012047.2:g.4993G>A
NG_012047.3:g.5000G>A