Canonical Allele Identifier: CA1363908976
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703529469

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345840del , CM000665.2:g.50345840del GRCh38
NC_000003.11:g.50383271del , CM000665.1:g.50383271del GRCh37
NC_000003.10:g.50358275del NCBI36
NG_023270.1:g.97del
NG_042828.1:g.4907del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-261del ENSP00000231749.3:n.-261del
XM_005265216.2:c.-389del XP_005265273.1:n.-389del