Canonical Allele Identifier: CA11025141
Gene:

Linked Data

ClinVar Variation Id: 869138
ClinVar RCV Id: RCV001078162
dbSNP Id: rs16944

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112837290A>G , CM000664.2:g.112837290A>G GRCh38
NC_000002.11:g.113594867A>G , CM000664.1:g.113594867A>G GRCh37
NC_000002.10:g.113311338A>G NCBI36
NG_008851.1:g.4490T>C