Canonical Allele Identifier: CA907891976
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1321015838
MyVariant Identifiers: chr3:g.50383159_50383165del (hg19) chr3:g.50345728_50345734del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345728_50345734del , CM000665.2:g.50345728_50345734del GRCh38
NC_000003.11:g.50383159_50383165del , CM000665.1:g.50383159_50383165del GRCh37
NC_000003.10:g.50358163_50358169del NCBI36
NG_023270.1:g.203_209del
NG_042828.1:g.5013_5019del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-155_-149del ENSP00000231749.3:n.-155_-149del
NM_001308379.1:c.-155_-149del NP_001295308.1:n.-155_-149del
NM_015896.3:c.-155_-149del NP_056980.2:n.-155_-149del
XM_005265216.2:c.-283_-277del XP_005265273.1:n.-283_-277del
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