Canonical Allele Identifier: CA1363908912
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345747A= , CM000665.2:g.50345747A= GRCh38
NC_000003.11:g.50383178A= , CM000665.1:g.50383178A= GRCh37
NC_000003.10:g.50358182A= NCBI36
NG_023270.1:g.190T=
NG_042828.1:g.5000T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-168T= ENSP00000231749.3:n.-168T=
XM_005265216.2:c.-296T= XP_005265273.1:n.-296T=