Canonical Allele Identifier: CA1363908953
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345806G= , CM000665.2:g.50345806G= GRCh38
NC_000003.11:g.50383237G= , CM000665.1:g.50383237G= GRCh37
NC_000003.10:g.50358241G= NCBI36
NG_023270.1:g.131C=
NG_042828.1:g.4941C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-227C= ENSP00000231749.3:n.-227C=
XM_005265216.2:c.-355C= XP_005265273.1:n.-355C=