Canonical Allele Identifier: CA907891653

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1259681612
• gnomAD v3: 3-50345387-G-T
• gnomAD v4: 3-50345387-G-T
• MyVariant Identifiers: chr3:g.50382818G>T (hg19) ; chr3:g.50345387G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345387G>T , CM000665.2:g.50345387G>T	GRCh38
NC_000003.11:g.50382818G>T , CM000665.1:g.50382818G>T	GRCh37
NC_000003.10:g.50357822G>T	NCBI36
NG_023270.1:g.550C>A
NG_042828.1:g.5360C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.92+101C>A MANE Select	ENSP00000231749.3:n.92+101C>A
ENST00000231749.7:c.92+101C>A	ENSP00000231749.3:n.92+101C>A
ENST00000360165.7:c.92+101C>A	ENSP00000353289.3:n.92+101C>A
ENST00000431869.1:c.92+101C>A	ENSP00000391545.1:n.92+101C>A
ENST00000442887.1:c.-38+148C>A	ENSP00000393687.1:n.-38+148C>A
ENST00000443080.5:c.92+101C>A	ENSP00000415661.1:n.92+101C>A
ENST00000468182.1:n.194+101C>A
NM_001308379.1:c.92+101C>A	NP_001295308.1:n.92+101C>A
NM_015896.2:c.92+101C>A	NP_056980.2:n.92+101C>A
NM_015896.3:c.92+101C>A	NP_056980.2:n.92+101C>A
XM_005265216.2:c.-37+101C>A	XP_005265273.1:n.-37+101C>A
XM_005265216.3:c.-37+101C>A	XP_005265273.1:n.-37+101C>A
NM_015896.4:c.92+101C>A MANE Select	NP_056980.2:n.92+101C>A
NM_001308379.2:c.92+101C>A	NP_001295308.1:n.92+101C>A