Canonical Allele Identifier: CA1363908982
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345850T= , CM000665.2:g.50345850T= GRCh38
NC_000003.11:g.50383281T= , CM000665.1:g.50383281T= GRCh37
NC_000003.10:g.50358285T= NCBI36
NG_023270.1:g.87A=
NG_042828.1:g.4897A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-271A= ENSP00000231749.3:n.-271A=
XM_005265216.2:c.-399A= XP_005265273.1:n.-399A=