Canonical Allele Identifier: CA51878383
Gene:

Linked Data

dbSNP Id: rs145127515
MyVariant Identifiers: chr2:g.88315911_88315912insGG (hg19) chr2:g.88016392_88016393insGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016392_88016393insGG , CM000664.2:g.88016392_88016393insGG GRCh38
NC_000002.11:g.88315911_88315912insGG , CM000664.1:g.88315911_88315912insGG GRCh37
NC_000002.10:g.88097026_88097027insGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.737_738insGG
XR_940336.3:n.737_738insGG
Search 100 bp 5'
Search 100 bp 3'