Canonical Allele Identifier: CA1573442284
Gene:

Linked Data

ClinVar Variation Id: 1011198
ClinVar RCV Id: RCV002241897
dbSNP Id: rs1185261719
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707424G>C , CM000667.2:g.112707424G>C GRCh38
NC_000005.9:g.112043121G>C , CM000667.1:g.112043121G>C GRCh37
NC_000005.8:g.112071020G>C NCBI36
NG_008481.4:g.19904G>C , LRG_130:g.19904G>C
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