Canonical Allele Identifier: CA725798502

Gene:

Linked Data

• dbSNP Id: rs1350418172
• MyVariant Identifiers: chr16:g.9343464_9343465insA (hg19) ; chr16:g.9249607_9249608insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249608dup , CM000678.2:g.9249608dup	GRCh38
NC_000016.9:g.9343465dup , CM000678.1:g.9343465dup	GRCh37
NC_000016.8:g.9250966dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64875dup