Canonical Allele Identifier: CA1363908961
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345821G= , CM000665.2:g.50345821G= GRCh38
NC_000003.11:g.50383252G= , CM000665.1:g.50383252G= GRCh37
NC_000003.10:g.50358256G= NCBI36
NG_023270.1:g.116C=
NG_042828.1:g.4926C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-242C= ENSP00000231749.3:n.-242C=
XM_005265216.2:c.-370C= XP_005265273.1:n.-370C=