Canonical Allele Identifier: CA675189409
Gene:

Linked Data

dbSNP Id: rs1436252033
MyVariant Identifiers: chr11:g.27505629_27505630insCG (hg19) chr11:g.27484082_27484083insCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484083_27484084dup , CM000673.2:g.27484083_27484084dup GRCh38
NC_000011.9:g.27505630_27505631dup , CM000673.1:g.27505630_27505631dup GRCh37
NC_000011.8:g.27462206_27462207dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.234_235dup
Search 100 bp 5'
Search 100 bp 3'