Canonical Allele Identifier: CA907892023

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1190651896
• gnomAD v3: 3-50345814-CG-C
• gnomAD v4: 3-50345814-CG-C
• MyVariant Identifiers: chr3:g.50383246del (hg19) ; chr3:g.50345815del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345815del , CM000665.2:g.50345815del	GRCh38
NC_000003.11:g.50383246del , CM000665.1:g.50383246del	GRCh37
NC_000003.10:g.50358250del	NCBI36
NG_023270.1:g.122del
NG_042828.1:g.4932del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-236del	ENSP00000231749.3:n.-236del
XM_005265216.2:c.-364del	XP_005265273.1:n.-364del