Canonical Allele Identifier: CA883240755
Gene:

Linked Data

dbSNP Id: rs1368469272
MyVariant Identifiers: chr19:g.51341059_51341060insG (hg19) chr19:g.50837803_50837804insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837806dup , CM000681.2:g.50837806dup GRCh38
NC_000019.9:g.51341062dup , CM000681.1:g.51341062dup GRCh37
NC_000019.8:g.56032874dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6513dup
NR_131205.1:n.230+6513dup
XR_936030.1:n.298+6513dup
XR_936031.1:n.298+6513dup
XR_936032.1:n.298+6513dup
XR_936033.1:n.294+6513dup
XR_936035.1:n.281+6513dup
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