Canonical Allele Identifier: CA185200434
Gene:

Linked Data

dbSNP Id: rs954537590
MyVariant Identifiers: chr8:g.123408343_123408344insA (hg19) chr8:g.122396104_122396105insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396111dup , CM000670.2:g.122396111dup GRCh38
NC_000008.10:g.123408350dup , CM000670.1:g.123408350dup GRCh37
NC_000008.9:g.123477531dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3067dup
XR_928599.3:n.152+3067dup
Search 100 bp 5'
Search 100 bp 3'