Canonical Allele Identifier: CA1573442161
Gene:

Linked Data

ClinVar Variation Id: 1021148
ClinVar RCV Id: RCV003652168
dbSNP Id: rs1750548429
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707327G>C , CM000667.2:g.112707327G>C GRCh38
NC_000005.9:g.112043024G>C , CM000667.1:g.112043024G>C GRCh37
NC_000005.8:g.112070923G>C NCBI36
NG_008481.4:g.19807G>C , LRG_130:g.19807G>C
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