Canonical Allele Identifier: CA433709016

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1489282193
• gnomAD v2: 3-50380371-A-G
• gnomAD v4: 3-50342940-A-G
• MyVariant Identifiers: chr3:g.50380371A>G (hg19) ; chr3:g.50342940A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342940A>G , CM000665.2:g.50342940A>G	GRCh38
NC_000003.11:g.50380371A>G , CM000665.1:g.50380371A>G	GRCh37
NC_000003.10:g.50355375A>G	NCBI36
NG_023270.1:g.2997T>C
NG_042828.1:g.7807T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.678T>C MANE Select	ENSP00000231749.3:p.Ser226=
ENST00000231749.7:c.678T>C	ENSP00000231749.3:p.Ser226=
ENST00000360165.7:c.599+178T>C	ENSP00000353289.3:n.599+178T>C
ENST00000442887.1:c.549T>C	ENSP00000393687.1:p.Ser183=
ENST00000443080.5:c.*430T>C	ENSP00000415661.1:n.*430T>C
ENST00000475688.1:n.229T>C
NM_001308379.1:c.599+178T>C	NP_001295308.1:n.599+178T>C
NM_015896.2:c.678T>C	NP_056980.2:p.Ser226=
NM_015896.3:c.678T>C	NP_056980.2:p.Ser226=
XM_005265216.2:c.441T>C	XP_005265273.1:p.Ser147=
XM_005265216.3:c.441T>C	XP_005265273.1:p.Ser147=
NM_015896.4:c.678T>C MANE Select	NP_056980.2:p.Ser226=
NM_001308379.2:c.599+178T>C	NP_001295308.1:n.599+178T>C