Canonical Allele Identifier: CA433710240

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1311676949
• gnomAD v2: 3-50382579-C-T
• gnomAD v4: 3-50345148-C-T
• MyVariant Identifiers: chr3:g.50382579C>T (hg19) ; chr3:g.50345148C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345148C>T , CM000665.2:g.50345148C>T	GRCh38
NC_000003.11:g.50382579C>T , CM000665.1:g.50382579C>T	GRCh37
NC_000003.10:g.50357583C>T	NCBI36
NG_023270.1:g.789G>A
NG_042828.1:g.5599G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.177G>A MANE Select	ENSP00000231749.3:p.Gln59=
ENST00000231749.7:c.177G>A	ENSP00000231749.3:p.Gln59=
ENST00000360165.7:c.177G>A	ENSP00000353289.3:p.Gln59=
ENST00000431869.1:c.*67G>A	ENSP00000391545.1:n.*67G>A
ENST00000442887.1:c.48G>A	ENSP00000393687.1:p.Gln16=
ENST00000443080.5:c.*67G>A	ENSP00000415661.1:n.*67G>A
ENST00000468182.1:n.279G>A
NM_001308379.1:c.177G>A	NP_001295308.1:p.Gln59=
NM_015896.2:c.177G>A	NP_056980.2:p.Gln59=
NM_015896.3:c.177G>A	NP_056980.2:p.Gln59=
XM_005265216.2:c.-37+340G>A	XP_005265273.1:n.-37+340G>A
XM_005265216.3:c.-37+340G>A	XP_005265273.1:n.-37+340G>A
NM_015896.4:c.177G>A MANE Select	NP_056980.2:p.Gln59=
NM_001308379.2:c.177G>A	NP_001295308.1:p.Gln59=