Canonical Allele Identifier: CA907891981
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1391088239
gnomAD v4: 3-50345735-C-T
MyVariant Identifiers: chr3:g.50383166C>T (hg19) chr3:g.50345735C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345735C>T , CM000665.2:g.50345735C>T GRCh38
NC_000003.11:g.50383166C>T , CM000665.1:g.50383166C>T GRCh37
NC_000003.10:g.50358170C>T NCBI36
NG_023270.1:g.202G>A
NG_042828.1:g.5012G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-156G>A ENSP00000231749.3:n.-156G>A
NM_001308379.1:c.-156G>A NP_001295308.1:n.-156G>A
NM_015896.3:c.-156G>A NP_056980.2:n.-156G>A
XM_005265216.2:c.-284G>A XP_005265273.1:n.-284G>A
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