Canonical Allele Identifier: CA2417333

Gene: ZMYND10

Linked Data

• ClinVar Variation Id: 3023491
• ClinVar RCV Id: RCV003882677
• dbSNP Id: rs775130379
• ExAC: 3:50382968 G / A
• gnomAD v2: 3-50382968-G-A
• gnomAD v4: 3-50345537-G-A
• MyVariant Identifiers: chr3:g.50382968G>A (hg19) ; chr3:g.50345537G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345537G>A , CM000665.2:g.50345537G>A	GRCh38
NC_000003.11:g.50382968G>A , CM000665.1:g.50382968G>A	GRCh37
NC_000003.10:g.50357972G>A	NCBI36
NG_023270.1:g.400C>T
NG_042828.1:g.5210C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000231749.8:c.43C>T MANE Select	ENSP00000231749.3:p.Leu15=
ENST00000231749.7:c.43C>T	ENSP00000231749.3:p.Leu15=
ENST00000360165.7:c.43C>T	ENSP00000353289.3:p.Leu15=
ENST00000431869.1:c.43C>T	ENSP00000391545.1:p.Leu15=
ENST00000442887.1:c.-40C>T	ENSP00000393687.1:n.-40C>T
ENST00000443080.5:c.43C>T	ENSP00000415661.1:p.Leu15=
ENST00000468182.1:n.145C>T
NM_001308379.1:c.43C>T	NP_001295308.1:p.Leu15=
NM_015896.2:c.43C>T	NP_056980.2:p.Leu15=
NM_015896.3:c.43C>T	NP_056980.2:p.Leu15=
XM_005265216.2:c.-86C>T	XP_005265273.1:n.-86C>T
XM_005265216.3:c.-86C>T	XP_005265273.1:n.-86C>T
NM_015896.4:c.43C>T MANE Select	NP_056980.2:p.Leu15=
NM_001308379.2:c.43C>T	NP_001295308.1:p.Leu15=