Canonical Allele Identifier: CA1363908909
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345740C= , CM000665.2:g.50345740C= GRCh38
NC_000003.11:g.50383171C= , CM000665.1:g.50383171C= GRCh37
NC_000003.10:g.50358175C= NCBI36
NG_023270.1:g.197G=
NG_042828.1:g.5007G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-161G= ENSP00000231749.3:n.-161G=
NM_001308379.1:c.-161G= NP_001295308.1:n.-161G=
NM_015896.3:c.-161G= NP_056980.2:n.-161G=
XM_005265216.2:c.-289G= XP_005265273.1:n.-289G=