Canonical Allele Identifier: CA1363908979
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345841T= , CM000665.2:g.50345841T= GRCh38
NC_000003.11:g.50383272T= , CM000665.1:g.50383272T= GRCh37
NC_000003.10:g.50358276T= NCBI36
NG_023270.1:g.96A=
NG_042828.1:g.4906A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-262A= ENSP00000231749.3:n.-262A=
XM_005265216.2:c.-390A= XP_005265273.1:n.-390A=