Canonical Allele Identifier: CA352941647

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1283465083
• gnomAD v2: 3-50380369-G-C
• gnomAD v4: 3-50342938-G-C
• MyVariant Identifiers: chr3:g.50380369G>C (hg19) ; chr3:g.50342938G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342938G>C , CM000665.2:g.50342938G>C	GRCh38
NC_000003.11:g.50380369G>C , CM000665.1:g.50380369G>C	GRCh37
NC_000003.10:g.50355373G>C	NCBI36
NG_023270.1:g.2999C>G
NG_042828.1:g.7809C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.680C>G MANE Select	ENSP00000231749.3:p.Pro227Arg
ENST00000231749.7:c.680C>G	ENSP00000231749.3:p.Pro227Arg
ENST00000360165.7:c.599+180C>G	ENSP00000353289.3:n.599+180C>G
ENST00000442887.1:c.551C>G	ENSP00000393687.1:p.Pro184Arg
ENST00000443080.5:c.*432C>G	ENSP00000415661.1:n.*432C>G
ENST00000475688.1:n.231C>G
NM_001308379.1:c.599+180C>G	NP_001295308.1:n.599+180C>G
NM_015896.2:c.680C>G	NP_056980.2:p.Pro227Arg
NM_015896.3:c.680C>G	NP_056980.2:p.Pro227Arg
XM_005265216.2:c.443C>G	XP_005265273.1:p.Pro148Arg
XM_005265216.3:c.443C>G	XP_005265273.1:p.Pro148Arg
NM_015896.4:c.680C>G MANE Select	NP_056980.2:p.Pro227Arg
NM_001308379.2:c.599+180C>G	NP_001295308.1:n.599+180C>G