Canonical Allele Identifier: CA907892028
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1310928638
MyVariant Identifiers: chr3:g.50383269T>A (hg19) chr3:g.50345838T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345838T>A , CM000665.2:g.50345838T>A GRCh38
NC_000003.11:g.50383269T>A , CM000665.1:g.50383269T>A GRCh37
NC_000003.10:g.50358273T>A NCBI36
NG_023270.1:g.99A>T
NG_042828.1:g.4909A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-259A>T ENSP00000231749.3:n.-259A>T
XM_005265216.2:c.-387A>T XP_005265273.1:n.-387A>T
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