Canonical Allele Identifier: CA907891986

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1422684578
• gnomAD v3: 3-50345741-CT-C
• gnomAD v4: 3-50345741-CT-C
• MyVariant Identifiers: chr3:g.50383173del (hg19) ; chr3:g.50345742del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345742del , CM000665.2:g.50345742del	GRCh38
NC_000003.11:g.50383173del , CM000665.1:g.50383173del	GRCh37
NC_000003.10:g.50358177del	NCBI36
NG_023270.1:g.195del
NG_042828.1:g.5005del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-163del	ENSP00000231749.3:n.-163del
NM_001308379.1:c.-163del	NP_001295308.1:n.-163del
NM_015896.3:c.-163del	NP_056980.2:n.-163del
XM_005265216.2:c.-291del	XP_005265273.1:n.-291del