Canonical Allele Identifier: CA857362191
Gene:

Linked Data

dbSNP Id: rs1369473360
MyVariant Identifiers: chr8:g.98281855_98281856insAC (hg19) chr8:g.97269627_97269628insAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269628_97269629dup , CM000670.2:g.97269628_97269629dup GRCh38
NC_000008.10:g.98281856_98281857dup , CM000670.1:g.98281856_98281857dup GRCh37
NC_000008.9:g.98351032_98351033dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149441_471+149442dup
Search 100 bp 5'
Search 100 bp 3'