Canonical Allele Identifier: CA543053888

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1199020121
• gnomAD v2: 3-50380303-C-T
• MyVariant Identifiers: chr3:g.50380303C>T (hg19) ; chr3:g.50342872C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342872C>T , CM000665.2:g.50342872C>T	GRCh38
NC_000003.11:g.50380303C>T , CM000665.1:g.50380303C>T	GRCh37
NC_000003.10:g.50355307C>T	NCBI36
NG_023270.1:g.3065G>A
NG_042828.1:g.7875G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+46G>A MANE Select	ENSP00000231749.3:n.700+46G>A
ENST00000231749.7:c.700+46G>A	ENSP00000231749.3:n.700+46G>A
ENST00000360165.7:c.600-217G>A	ENSP00000353289.3:n.600-217G>A
ENST00000442887.1:c.571+46G>A	ENSP00000393687.1:n.571+46G>A
ENST00000443080.5:c.*452+46G>A	ENSP00000415661.1:n.*452+46G>A
ENST00000475688.1:n.297G>A
NM_001308379.1:c.600-217G>A	NP_001295308.1:n.600-217G>A
NM_015896.2:c.700+46G>A	NP_056980.2:n.700+46G>A
NM_015896.3:c.700+46G>A	NP_056980.2:n.700+46G>A
XM_005265216.2:c.463+46G>A	XP_005265273.1:n.463+46G>A
XM_005265216.3:c.463+46G>A	XP_005265273.1:n.463+46G>A
NM_015896.4:c.700+46G>A MANE Select	NP_056980.2:n.700+46G>A
NM_001308379.2:c.600-217G>A	NP_001295308.1:n.600-217G>A