Canonical Allele Identifier: CA725798432
Gene:

Linked Data

dbSNP Id: rs1293884157
gnomAD v3: 16-9249459-C-CT
gnomAD v4: 16-9249459-C-CT
MyVariant Identifiers: chr16:g.9343316_9343317insT (hg19) chr16:g.9249459_9249460insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249460dup , CM000678.2:g.9249460dup GRCh38
NC_000016.9:g.9343317dup , CM000678.1:g.9343317dup GRCh37
NC_000016.8:g.9250818dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64727dup
Search 100 bp 5'
Search 100 bp 3'