Canonical Allele Identifier: CA305052888
Gene:

Linked Data

dbSNP Id: rs760248002
gnomAD v3: 19-9127268-C-CTTCT
gnomAD v4: 19-9127268-C-CTTCT
MyVariant Identifiers: chr19:g.9237944_9237945insTTCT (hg19) chr19:g.9127268_9127269insTTCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9127281_9127284dup , CM000681.2:g.9127281_9127284dup GRCh38
NC_000019.9:g.9237957_9237960dup , CM000681.1:g.9237957_9237960dup GRCh37
NC_000019.8:g.9098957_9098960dup NCBI36
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