Canonical Allele Identifier: CA2756211948
Gene: ZMYND10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345910C>T , CM000665.2:g.50345910C>T GRCh38
NC_000003.11:g.50383341C>T , CM000665.1:g.50383341C>T GRCh37
NC_000003.10:g.50358345C>T NCBI36
NG_023270.1:g.27G>A
NG_042828.1:g.4837G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-331G>A ENSP00000231749.3:n.-331G>A
XM_005265216.2:c.-459G>A XP_005265273.1:n.-459G>A
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