Canonical Allele Identifier: CA543053905

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1215328411
• gnomAD v2: 3-50380650-A-G
• gnomAD v3: 3-50343219-A-G
• gnomAD v4: 3-50343219-A-G
• MyVariant Identifiers: chr3:g.50380650A>G (hg19) ; chr3:g.50343219A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343219A>G , CM000665.2:g.50343219A>G	GRCh38
NC_000003.11:g.50380650A>G , CM000665.1:g.50380650A>G	GRCh37
NC_000003.10:g.50355654A>G	NCBI36
NG_023270.1:g.2718T>C
NG_042828.1:g.7528T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.511-13T>C MANE Select	ENSP00000231749.3:n.511-13T>C
ENST00000231749.7:c.511-13T>C	ENSP00000231749.3:n.511-13T>C
ENST00000360165.7:c.511-13T>C	ENSP00000353289.3:n.511-13T>C
ENST00000442887.1:c.382-13T>C	ENSP00000393687.1:n.382-13T>C
ENST00000443080.5:c.*263-13T>C	ENSP00000415661.1:n.*263-13T>C
ENST00000478269.5:n.583T>C
NM_001308379.1:c.511-13T>C	NP_001295308.1:n.511-13T>C
NM_015896.2:c.511-13T>C	NP_056980.2:n.511-13T>C
NM_015896.3:c.511-13T>C	NP_056980.2:n.511-13T>C
XM_005265216.2:c.274-13T>C	XP_005265273.1:n.274-13T>C
XM_005265216.3:c.274-13T>C	XP_005265273.1:n.274-13T>C
NM_015896.4:c.511-13T>C MANE Select	NP_056980.2:n.511-13T>C
NM_001308379.2:c.511-13T>C	NP_001295308.1:n.511-13T>C