Canonical Allele Identifier: CA1363908959
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345818T= , CM000665.2:g.50345818T= GRCh38
NC_000003.11:g.50383249T= , CM000665.1:g.50383249T= GRCh37
NC_000003.10:g.50358253T= NCBI36
NG_023270.1:g.119A=
NG_042828.1:g.4929A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-239A= ENSP00000231749.3:n.-239A=
XM_005265216.2:c.-367A= XP_005265273.1:n.-367A=