Canonical Allele Identifier: CA352945985

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1439364366
• gnomAD v2: 3-50382941-G-C
• gnomAD v4: 3-50345510-G-C
• MyVariant Identifiers: chr3:g.50382941G>C (hg19) ; chr3:g.50345510G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345510G>C , CM000665.2:g.50345510G>C	GRCh38
NC_000003.11:g.50382941G>C , CM000665.1:g.50382941G>C	GRCh37
NC_000003.10:g.50357945G>C	NCBI36
NG_023270.1:g.427C>G
NG_042828.1:g.5237C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.70C>G MANE Select	ENSP00000231749.3:p.Leu24Val
ENST00000231749.7:c.70C>G	ENSP00000231749.3:p.Leu24Val
ENST00000360165.7:c.70C>G	ENSP00000353289.3:p.Leu24Val
ENST00000431869.1:c.70C>G	ENSP00000391545.1:p.Leu24Val
ENST00000442887.1:c.-38+25C>G	ENSP00000393687.1:n.-38+25C>G
ENST00000443080.5:c.70C>G	ENSP00000415661.1:p.Leu24Val
ENST00000468182.1:n.172C>G
NM_001308379.1:c.70C>G	NP_001295308.1:p.Leu24Val
NM_015896.2:c.70C>G	NP_056980.2:p.Leu24Val
NM_015896.3:c.70C>G	NP_056980.2:p.Leu24Val
XM_005265216.2:c.-59C>G	XP_005265273.1:n.-59C>G
XM_005265216.3:c.-59C>G	XP_005265273.1:n.-59C>G
NM_015896.4:c.70C>G MANE Select	NP_056980.2:p.Leu24Val
NM_001308379.2:c.70C>G	NP_001295308.1:p.Leu24Val