Canonical Allele Identifier: CA1363908891

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1703524670

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345720A>G , CM000665.2:g.50345720A>G	GRCh38
NC_000003.11:g.50383151A>G , CM000665.1:g.50383151A>G	GRCh37
NC_000003.10:g.50358155A>G	NCBI36
NG_023270.1:g.217T>C
NG_042828.1:g.5027T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-141T>C MANE Select	ENSP00000231749.3:n.-141T>C
ENST00000231749.7:c.-141T>C	ENSP00000231749.3:n.-141T>C
ENST00000360165.7:c.-141T>C	ENSP00000353289.3:n.-141T>C
ENST00000431869.1:c.-141T>C	ENSP00000391545.1:n.-141T>C
ENST00000442887.1:c.-223T>C	ENSP00000393687.1:n.-223T>C
NM_001308379.1:c.-141T>C	NP_001295308.1:n.-141T>C
NM_015896.2:c.-141T>C	NP_056980.2:n.-141T>C
NM_015896.3:c.-141T>C	NP_056980.2:n.-141T>C
XM_005265216.2:c.-269T>C	XP_005265273.1:n.-269T>C
NM_015896.4:c.-141T>C MANE Select	NP_056980.2:n.-141T>C
NM_001308379.2:c.-141T>C	NP_001295308.1:n.-141T>C