Canonical Allele Identifier: CA2417293

Gene: ZMYND10

Linked Data

• dbSNP Id: rs765025165
• ExAC: 3:50382561 A / G
• gnomAD v2: 3-50382561-A-G
• gnomAD v4: 3-50345130-A-G
• MyVariant Identifiers: chr3:g.50382561A>G (hg19) ; chr3:g.50345130A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345130A>G , CM000665.2:g.50345130A>G	GRCh38
NC_000003.11:g.50382561A>G , CM000665.1:g.50382561A>G	GRCh37
NC_000003.10:g.50357565A>G	NCBI36
NG_023270.1:g.807T>C
NG_042828.1:g.5617T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.195T>C MANE Select	ENSP00000231749.3:p.His65=
ENST00000231749.7:c.195T>C	ENSP00000231749.3:p.His65=
ENST00000360165.7:c.195T>C	ENSP00000353289.3:p.His65=
ENST00000431869.1:c.*85T>C	ENSP00000391545.1:n.*85T>C
ENST00000442887.1:c.66T>C	ENSP00000393687.1:p.His22=
ENST00000443080.5:c.*85T>C	ENSP00000415661.1:n.*85T>C
ENST00000468182.1:n.297T>C
NM_001308379.1:c.195T>C	NP_001295308.1:p.His65=
NM_015896.2:c.195T>C	NP_056980.2:p.His65=
NM_015896.3:c.195T>C	NP_056980.2:p.His65=
XM_005265216.2:c.-37+358T>C	XP_005265273.1:n.-37+358T>C
XM_005265216.3:c.-37+358T>C	XP_005265273.1:n.-37+358T>C
NM_015896.4:c.195T>C MANE Select	NP_056980.2:p.His65=
NM_001308379.2:c.195T>C	NP_001295308.1:p.His65=