Canonical Allele Identifier: CA1363908992
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345870G= , CM000665.2:g.50345870G= GRCh38
NC_000003.11:g.50383301G= , CM000665.1:g.50383301G= GRCh37
NC_000003.10:g.50358305G= NCBI36
NG_023270.1:g.67C=
NG_042828.1:g.4877C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-291C= ENSP00000231749.3:n.-291C=
XM_005265216.2:c.-419C= XP_005265273.1:n.-419C=