Canonical Allele Identifier: CA883240715
Gene:

Linked Data

dbSNP Id: rs1328703326
gnomAD v3: 19-50837501-A-AT
gnomAD v4: 19-50837501-A-AT
MyVariant Identifiers: chr19:g.51340757_51340758insT (hg19) chr19:g.50837501_50837502insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837502dup , CM000681.2:g.50837502dup GRCh38
NC_000019.9:g.51340758dup , CM000681.1:g.51340758dup GRCh37
NC_000019.8:g.56032570dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6209dup
NR_131205.1:n.230+6209dup
XR_936030.1:n.298+6209dup
XR_936031.1:n.298+6209dup
XR_936032.1:n.298+6209dup
XR_936033.1:n.294+6209dup
XR_936035.1:n.281+6209dup
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