Canonical Allele Identifier: CA1363908902
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345735C= , CM000665.2:g.50345735C= GRCh38
NC_000003.11:g.50383166C= , CM000665.1:g.50383166C= GRCh37
NC_000003.10:g.50358170C= NCBI36
NG_023270.1:g.202G=
NG_042828.1:g.5012G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-156G= ENSP00000231749.3:n.-156G=
NM_001308379.1:c.-156G= NP_001295308.1:n.-156G=
NM_015896.3:c.-156G= NP_056980.2:n.-156G=
XM_005265216.2:c.-284G= XP_005265273.1:n.-284G=