Canonical Allele Identifier: CA1573442294
Gene:

Linked Data

ClinVar Variation Id: 1018804
ClinVar RCV Id: RCV002543744
dbSNP Id: rs781399686

Genomic Alleles

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