Canonical Allele Identifier: CA300391563
Gene:

Linked Data

dbSNP Id: rs748489476
MyVariant Identifiers: chr18:g.47172334_47172335insG (hg19) chr18:g.49645964_49645965insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645969dup , CM000680.2:g.49645969dup GRCh38
NC_000018.9:g.47172339dup , CM000680.1:g.47172339dup GRCh37
NC_000018.8:g.45426337dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935461.1:n.162-16065dup
XR_001753446.1:n.898-16065dup
Search 100 bp 5'
Search 100 bp 3'