Canonical Allele Identifier: CA2573138744
Gene:

Linked Data

ClinVar Variation Id: 1435210
ClinVar RCV Id: RCV003772887
dbSNP Id: rs1243549213
gnomAD v4: 5-112707378-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707378G>T , CM000667.2:g.112707378G>T GRCh38
NC_000005.9:g.112043075G>T , CM000667.1:g.112043075G>T GRCh37
NC_000005.8:g.112070974G>T NCBI36
NG_008481.4:g.19858G>T , LRG_130:g.19858G>T
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