Canonical Allele Identifier: CA2417157

Gene: ZMYND10

Linked Data

• dbSNP Id: rs763590048
• ExAC: 3:50380494 C / T
• gnomAD v2: 3-50380494-C-T
• gnomAD v3: 3-50343063-C-T
• gnomAD v4: 3-50343063-C-T
• MyVariant Identifiers: chr3:g.50380494C>T (hg19) ; chr3:g.50343063C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343063C>T , CM000665.2:g.50343063C>T	GRCh38
NC_000003.11:g.50380494C>T , CM000665.1:g.50380494C>T	GRCh37
NC_000003.10:g.50355498C>T	NCBI36
NG_023270.1:g.2874G>A
NG_042828.1:g.7684G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.600-45G>A MANE Select	ENSP00000231749.3:n.600-45G>A
ENST00000231749.7:c.600-45G>A	ENSP00000231749.3:n.600-45G>A
ENST00000360165.7:c.599+55G>A	ENSP00000353289.3:n.599+55G>A
ENST00000442887.1:c.471-45G>A	ENSP00000393687.1:n.471-45G>A
ENST00000443080.5:c.*352-45G>A	ENSP00000415661.1:n.*352-45G>A
ENST00000475688.1:n.106G>A
NM_001308379.1:c.599+55G>A	NP_001295308.1:n.599+55G>A
NM_015896.2:c.600-45G>A	NP_056980.2:n.600-45G>A
NM_015896.3:c.600-45G>A	NP_056980.2:n.600-45G>A
XM_005265216.2:c.363-45G>A	XP_005265273.1:n.363-45G>A
XM_005265216.3:c.363-45G>A	XP_005265273.1:n.363-45G>A
NM_015896.4:c.600-45G>A MANE Select	NP_056980.2:n.600-45G>A
NM_001308379.2:c.599+55G>A	NP_001295308.1:n.599+55G>A