Canonical Allele Identifier: CA1363908947
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345799G= , CM000665.2:g.50345799G= GRCh38
NC_000003.11:g.50383230G= , CM000665.1:g.50383230G= GRCh37
NC_000003.10:g.50358234G= NCBI36
NG_023270.1:g.138C=
NG_042828.1:g.4948C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-220C= ENSP00000231749.3:n.-220C=
XM_005265216.2:c.-348C= XP_005265273.1:n.-348C=