Canonical Allele Identifier: CA542854449

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1382168427
• gnomAD v2: 3-50382671-A-C
• gnomAD v4: 3-50345240-A-C
• MyVariant Identifiers: chr3:g.50382671A>C (hg19) ; chr3:g.50345240A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345240A>C , CM000665.2:g.50345240A>C	GRCh38
NC_000003.11:g.50382671A>C , CM000665.1:g.50382671A>C	GRCh37
NC_000003.10:g.50357675A>C	NCBI36
NG_023270.1:g.697T>G
NG_042828.1:g.5507T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.93-8T>G MANE Select	ENSP00000231749.3:n.93-8T>G
ENST00000231749.7:c.93-8T>G	ENSP00000231749.3:n.93-8T>G
ENST00000360165.7:c.93-8T>G	ENSP00000353289.3:n.93-8T>G
ENST00000431869.1:c.93-4T>G	ENSP00000391545.1:n.93-4T>G
ENST00000442887.1:c.-37-8T>G	ENSP00000393687.1:n.-37-8T>G
ENST00000443080.5:c.93-4T>G	ENSP00000415661.1:n.93-4T>G
ENST00000468182.1:n.195-8T>G
NM_001308379.1:c.93-8T>G	NP_001295308.1:n.93-8T>G
NM_015896.2:c.93-8T>G	NP_056980.2:n.93-8T>G
NM_015896.3:c.93-8T>G	NP_056980.2:n.93-8T>G
XM_005265216.2:c.-37+248T>G	XP_005265273.1:n.-37+248T>G
XM_005265216.3:c.-37+248T>G	XP_005265273.1:n.-37+248T>G
NM_015896.4:c.93-8T>G MANE Select	NP_056980.2:n.93-8T>G
NM_001308379.2:c.93-8T>G	NP_001295308.1:n.93-8T>G