Canonical Allele Identifier: CA1363908937
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703526771

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345789del , CM000665.2:g.50345789del GRCh38
NC_000003.11:g.50383220del , CM000665.1:g.50383220del GRCh37
NC_000003.10:g.50358224del NCBI36
NG_023270.1:g.150del
NG_042828.1:g.4960del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-208del ENSP00000231749.3:n.-208del
XM_005265216.2:c.-336del XP_005265273.1:n.-336del