Canonical Allele Identifier: CA191701718
Gene:

Linked Data

dbSNP Id: rs377685777
MyVariant Identifiers: chr9:g.25551508_25551509insCTTTTACAGCCTTTT (hg19) chr9:g.25551510_25551511insCTTTTACAGCCTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551510_25551511insCTTTTACAGCCTTTT , CM000671.2:g.25551510_25551511insCTTTTACAGCCTTTT GRCh38
NC_000009.11:g.25551508_25551509insCTTTTACAGCCTTTT , CM000671.1:g.25551508_25551509insCTTTTACAGCCTTTT GRCh37
NC_000009.10:g.25541508_25541509insCTTTTACAGCCTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-939_50-938insAAAAGGCTGTAAAAG
XR_929525.2:n.674-939_674-938insAAAAGGCTGTAAAAG
Search 100 bp 5'
Search 100 bp 3'