Canonical Allele Identifier: CA2665848567
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345738-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345738C>A , CM000665.2:g.50345738C>A GRCh38
NC_000003.11:g.50383169C>A , CM000665.1:g.50383169C>A GRCh37
NC_000003.10:g.50358173C>A NCBI36
NG_023270.1:g.199G>T
NG_042828.1:g.5009G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-159G>T ENSP00000231749.3:n.-159G>T
NM_001308379.1:c.-159G>T NP_001295308.1:n.-159G>T
NM_015896.3:c.-159G>T NP_056980.2:n.-159G>T
XM_005265216.2:c.-287G>T XP_005265273.1:n.-287G>T
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