Canonical Allele Identifier: CA2417299

Gene: ZMYND10

Linked Data

• dbSNP Id: rs780519054
• ExAC: 3:50382617 T / C
• gnomAD v2: 3-50382617-T-C
• gnomAD v4: 3-50345186-T-C
• MyVariant Identifiers: chr3:g.50382617T>C (hg19) ; chr3:g.50345186T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345186T>C , CM000665.2:g.50345186T>C	GRCh38
NC_000003.11:g.50382617T>C , CM000665.1:g.50382617T>C	GRCh37
NC_000003.10:g.50357621T>C	NCBI36
NG_023270.1:g.751A>G
NG_042828.1:g.5561A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.139A>G MANE Select	ENSP00000231749.3:p.Ile47Val
ENST00000231749.7:c.139A>G	ENSP00000231749.3:p.Ile47Val
ENST00000360165.7:c.139A>G	ENSP00000353289.3:p.Ile47Val
ENST00000431869.1:c.*29A>G	ENSP00000391545.1:n.*29A>G
ENST00000442887.1:c.10A>G	ENSP00000393687.1:p.Ile4Val
ENST00000443080.5:c.*29A>G	ENSP00000415661.1:n.*29A>G
ENST00000468182.1:n.241A>G
NM_001308379.1:c.139A>G	NP_001295308.1:p.Ile47Val
NM_015896.2:c.139A>G	NP_056980.2:p.Ile47Val
NM_015896.3:c.139A>G	NP_056980.2:p.Ile47Val
XM_005265216.2:c.-37+302A>G	XP_005265273.1:n.-37+302A>G
XM_005265216.3:c.-37+302A>G	XP_005265273.1:n.-37+302A>G
NM_015896.4:c.139A>G MANE Select	NP_056980.2:p.Ile47Val
NM_001308379.2:c.139A>G	NP_001295308.1:p.Ile47Val