Canonical Allele Identifier: CA124924659
Gene:

Linked Data

ClinVar Variation Id: 1379550
ClinVar RCV Id: RCV003745386
dbSNP Id: rs781399686

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707435G>T , CM000667.2:g.112707435G>T GRCh38
NC_000005.9:g.112043132G>T , CM000667.1:g.112043132G>T GRCh37
NC_000005.8:g.112071031G>T NCBI36
NG_008481.4:g.19915G>T , LRG_130:g.19915G>T