Canonical Allele Identifier: CA907891982
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1166790255
gnomAD v3: 3-50345736-C-A
gnomAD v4: 3-50345736-C-A
MyVariant Identifiers: chr3:g.50383167C>A (hg19) chr3:g.50345736C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345736C>A , CM000665.2:g.50345736C>A GRCh38
NC_000003.11:g.50383167C>A , CM000665.1:g.50383167C>A GRCh37
NC_000003.10:g.50358171C>A NCBI36
NG_023270.1:g.201G>T
NG_042828.1:g.5011G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-157G>T ENSP00000231749.3:n.-157G>T
NM_001308379.1:c.-157G>T NP_001295308.1:n.-157G>T
NM_015896.3:c.-157G>T NP_056980.2:n.-157G>T
XM_005265216.2:c.-285G>T XP_005265273.1:n.-285G>T
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