Canonical Allele Identifier: CA2665848800
Gene: ZMYND10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345886del , CM000665.2:g.50345886del GRCh38
NC_000003.11:g.50383317del , CM000665.1:g.50383317del GRCh37
NC_000003.10:g.50358321del NCBI36
NG_023270.1:g.51del
NG_042828.1:g.4861del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-307del ENSP00000231749.3:n.-307del
XM_005265216.2:c.-435del XP_005265273.1:n.-435del