Canonical Allele Identifier: CA433711833

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50345681-C-G
• MyVariant Identifiers: chr3:g.50383112C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345681C>G , CM000665.2:g.50345681C>G	GRCh38
NC_000003.11:g.50383112C>G , CM000665.1:g.50383112C>G	GRCh37
NC_000003.10:g.50358116C>G	NCBI36
NG_023270.1:g.256G>C
NG_042828.1:g.5066G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-102G>C MANE Select	ENSP00000231749.3:n.-102G>C
ENST00000231749.7:c.-102G>C	ENSP00000231749.3:n.-102G>C
ENST00000360165.7:c.-102G>C	ENSP00000353289.3:n.-102G>C
ENST00000431869.1:c.-102G>C	ENSP00000391545.1:n.-102G>C
ENST00000442887.1:c.-184G>C	ENSP00000393687.1:n.-184G>C
ENST00000468182.1:n.1G>C
NM_001308379.1:c.-102G>C	NP_001295308.1:n.-102G>C
NM_015896.2:c.-102G>C	NP_056980.2:n.-102G>C
NM_015896.3:c.-102G>C	NP_056980.2:n.-102G>C
XM_005265216.2:c.-230G>C	XP_005265273.1:n.-230G>C
XM_005265216.3:c.-230G>C	XP_005265273.1:n.-230G>C
NM_015896.4:c.-102G>C MANE Select	NP_056980.2:n.-102G>C
NM_001308379.2:c.-102G>C	NP_001295308.1:n.-102G>C