Canonical Allele Identifier: CA2665848569
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345740-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345740C>G , CM000665.2:g.50345740C>G GRCh38
NC_000003.11:g.50383171C>G , CM000665.1:g.50383171C>G GRCh37
NC_000003.10:g.50358175C>G NCBI36
NG_023270.1:g.197G>C
NG_042828.1:g.5007G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-161G>C ENSP00000231749.3:n.-161G>C
NM_001308379.1:c.-161G>C NP_001295308.1:n.-161G>C
NM_015896.3:c.-161G>C NP_056980.2:n.-161G>C
XM_005265216.2:c.-289G>C XP_005265273.1:n.-289G>C
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