Canonical Allele Identifier: CA433711327

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1212617932
• gnomAD v2: 3-50383017-G-A
• gnomAD v4: 3-50345586-G-A
• MyVariant Identifiers: chr3:g.50383017G>A (hg19) ; chr3:g.50345586G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345586G>A , CM000665.2:g.50345586G>A	GRCh38
NC_000003.11:g.50383017G>A , CM000665.1:g.50383017G>A	GRCh37
NC_000003.10:g.50358021G>A	NCBI36
NG_023270.1:g.351C>T
NG_042828.1:g.5161C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-7C>T MANE Select	ENSP00000231749.3:n.-7C>T
ENST00000231749.7:c.-7C>T	ENSP00000231749.3:n.-7C>T
ENST00000360165.7:c.-7C>T	ENSP00000353289.3:n.-7C>T
ENST00000431869.1:c.-7C>T	ENSP00000391545.1:n.-7C>T
ENST00000442887.1:c.-89C>T	ENSP00000393687.1:n.-89C>T
ENST00000443080.5:c.-7C>T	ENSP00000415661.1:n.-7C>T
ENST00000468182.1:n.96C>T
NM_001308379.1:c.-7C>T	NP_001295308.1:n.-7C>T
NM_015896.2:c.-7C>T	NP_056980.2:n.-7C>T
NM_015896.3:c.-7C>T	NP_056980.2:n.-7C>T
XM_005265216.2:c.-135C>T	XP_005265273.1:n.-135C>T
XM_005265216.3:c.-135C>T	XP_005265273.1:n.-135C>T
NM_015896.4:c.-7C>T MANE Select	NP_056980.2:n.-7C>T
NM_001308379.2:c.-7C>T	NP_001295308.1:n.-7C>T