Canonical Allele Identifier: CA2665848561
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345733-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345733A>C , CM000665.2:g.50345733A>C GRCh38
NC_000003.11:g.50383164A>C , CM000665.1:g.50383164A>C GRCh37
NC_000003.10:g.50358168A>C NCBI36
NG_023270.1:g.204T>G
NG_042828.1:g.5014T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-154T>G ENSP00000231749.3:n.-154T>G
NM_001308379.1:c.-154T>G NP_001295308.1:n.-154T>G
NM_015896.3:c.-154T>G NP_056980.2:n.-154T>G
XM_005265216.2:c.-282T>G XP_005265273.1:n.-282T>G
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