Canonical Allele Identifier: CA2665848564
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345734-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345734G>A , CM000665.2:g.50345734G>A GRCh38
NC_000003.11:g.50383165G>A , CM000665.1:g.50383165G>A GRCh37
NC_000003.10:g.50358169G>A NCBI36
NG_023270.1:g.203C>T
NG_042828.1:g.5013C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-155C>T ENSP00000231749.3:n.-155C>T
NM_001308379.1:c.-155C>T NP_001295308.1:n.-155C>T
NM_015896.3:c.-155C>T NP_056980.2:n.-155C>T
XM_005265216.2:c.-283C>T XP_005265273.1:n.-283C>T
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