Canonical Allele Identifier: CA2702794007

Gene: ZMYND10

Linked Data

• dbSNP Id: rs2109357928

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343267C>G , CM000665.2:g.50343267C>G	GRCh38
NC_000003.11:g.50380698C>G , CM000665.1:g.50380698C>G	GRCh37
NC_000003.10:g.50355702C>G	NCBI36
NG_023270.1:g.2670G>C
NG_042828.1:g.7480G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.510+40G>C MANE Select	ENSP00000231749.3:n.510+40G>C
ENST00000231749.7:c.510+40G>C	ENSP00000231749.3:n.510+40G>C
ENST00000360165.7:c.510+40G>C	ENSP00000353289.3:n.510+40G>C
ENST00000442887.1:c.381+40G>C	ENSP00000393687.1:n.381+40G>C
ENST00000443080.5:c.*263-61G>C	ENSP00000415661.1:n.*263-61G>C
ENST00000478269.5:n.535G>C
NM_001308379.1:c.510+40G>C	NP_001295308.1:n.510+40G>C
NM_015896.2:c.510+40G>C	NP_056980.2:n.510+40G>C
NM_015896.3:c.510+40G>C	NP_056980.2:n.510+40G>C
XM_005265216.2:c.273+40G>C	XP_005265273.1:n.273+40G>C
XM_005265216.3:c.273+40G>C	XP_005265273.1:n.273+40G>C
NM_015896.4:c.510+40G>C MANE Select	NP_056980.2:n.510+40G>C
NM_001308379.2:c.510+40G>C	NP_001295308.1:n.510+40G>C