Canonical Allele Identifier: CA74634796

Gene: ZMYND10

Linked Data

• dbSNP Id: rs748970966
• MyVariant Identifiers: chr3:g.50383249_50383250insA (hg19) ; chr3:g.50345818_50345819insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345819dup , CM000665.2:g.50345819dup	GRCh38
NC_000003.11:g.50383250dup , CM000665.1:g.50383250dup	GRCh37
NC_000003.10:g.50358254dup	NCBI36
NG_023270.1:g.118dup
NG_042828.1:g.4928dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-240dup	ENSP00000231749.3:n.-240dup
XM_005265216.2:c.-368dup	XP_005265273.1:n.-368dup