Canonical Allele Identifier: CA191701719
Gene:

Linked Data

dbSNP Id: rs377685777
gnomAD v2: 9-25551508-C-CTGTAAAACAGCCTTTTACAGCCTTTT
gnomAD v3: 9-25551510-C-CTGTAAAACAGCCTTTTACAGCCTTTT
gnomAD v4: 9-25551510-C-CTGTAAAACAGCCTTTTACAGCCTTTT
MyVariant Identifiers: chr9:g.25551508_25551509insTGTAAAACAGCCTTTTACAGCCTTTT (hg19) chr9:g.25551510_25551511insTGTAAAACAGCCTTTTACAGCCTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551510_25551511insTGTAAAACAGCCTTTTACAGCCTTTT , CM000671.2:g.25551510_25551511insTGTAAAACAGCCTTTTACAGCCTTTT GRCh38
NC_000009.11:g.25551508_25551509insTGTAAAACAGCCTTTTACAGCCTTTT , CM000671.1:g.25551508_25551509insTGTAAAACAGCCTTTTACAGCCTTTT GRCh37
NC_000009.10:g.25541508_25541509insTGTAAAACAGCCTTTTACAGCCTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-939_50-938insAAAAGGCTGTAAAAGGCTGTTTTACA
XR_929525.2:n.674-939_674-938insAAAAGGCTGTAAAAGGCTGTTTTACA
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