Canonical Allele Identifier: CA2665848783
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345874-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345874C>T , CM000665.2:g.50345874C>T GRCh38
NC_000003.11:g.50383305C>T , CM000665.1:g.50383305C>T GRCh37
NC_000003.10:g.50358309C>T NCBI36
NG_023270.1:g.63G>A
NG_042828.1:g.4873G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-295G>A ENSP00000231749.3:n.-295G>A
XM_005265216.2:c.-423G>A XP_005265273.1:n.-423G>A
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