Canonical Allele Identifier: CA1363909001
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345885C= , CM000665.2:g.50345885C= GRCh38
NC_000003.11:g.50383316C= , CM000665.1:g.50383316C= GRCh37
NC_000003.10:g.50358320C= NCBI36
NG_023270.1:g.52G=
NG_042828.1:g.4862G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-306G= ENSP00000231749.3:n.-306G=
XM_005265216.2:c.-434G= XP_005265273.1:n.-434G=