Canonical Allele Identifier: CA1573442182
Gene:

Linked Data

ClinVar Variation Id: 1021742
ClinVar RCV Id: RCV003538695
dbSNP Id: rs1750550286
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707345T>C , CM000667.2:g.112707345T>C GRCh38
NC_000005.9:g.112043042T>C , CM000667.1:g.112043042T>C GRCh37
NC_000005.8:g.112070941T>C NCBI36
NG_008481.4:g.19825T>C , LRG_130:g.19825T>C
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