Canonical Allele Identifier: CA124924639
Gene:

Linked Data

ClinVar Variation Id: 537680
ClinVar RCV Id: RCV003534537
dbSNP Id: rs1012461653

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707412A>C , CM000667.2:g.112707412A>C GRCh38
NC_000005.9:g.112043109A>C , CM000667.1:g.112043109A>C GRCh37
NC_000005.8:g.112071008A>C NCBI36
NG_008481.4:g.19892A>C , LRG_130:g.19892A>C