Canonical Allele Identifier: CA2417125

Gene: ZMYND10

Linked Data

• ClinVar Variation Id: 2910885
• ClinVar RCV Id: RCV003651782
• dbSNP Id: rs191853356
• ExAC: 3:50380334 G / C
• gnomAD v2: 3-50380334-G-C
• gnomAD v3: 3-50342903-G-C
• gnomAD v4: 3-50342903-G-C
• MyVariant Identifiers: chr3:g.50380334G>C (hg19) ; chr3:g.50342903G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342903G>C , CM000665.2:g.50342903G>C	GRCh38
NC_000003.11:g.50380334G>C , CM000665.1:g.50380334G>C	GRCh37
NC_000003.10:g.50355338G>C	NCBI36
NG_023270.1:g.3034C>G
NG_042828.1:g.7844C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+15C>G MANE Select	ENSP00000231749.3:n.700+15C>G
ENST00000231749.7:c.700+15C>G	ENSP00000231749.3:n.700+15C>G
ENST00000360165.7:c.599+215C>G	ENSP00000353289.3:n.599+215C>G
ENST00000442887.1:c.571+15C>G	ENSP00000393687.1:n.571+15C>G
ENST00000443080.5:c.*452+15C>G	ENSP00000415661.1:n.*452+15C>G
ENST00000475688.1:n.266C>G
NM_001308379.1:c.599+215C>G	NP_001295308.1:n.599+215C>G
NM_015896.2:c.700+15C>G	NP_056980.2:n.700+15C>G
NM_015896.3:c.700+15C>G	NP_056980.2:n.700+15C>G
XM_005265216.2:c.463+15C>G	XP_005265273.1:n.463+15C>G
XM_005265216.3:c.463+15C>G	XP_005265273.1:n.463+15C>G
NM_015896.4:c.700+15C>G MANE Select	NP_056980.2:n.700+15C>G
NM_001308379.2:c.599+215C>G	NP_001295308.1:n.599+215C>G