Canonical Allele Identifier: CA907889696

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1179782350
• gnomAD v4: 3-50342727-C-T
• MyVariant Identifiers: chr3:g.50380158C>T (hg19) ; chr3:g.50342727C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342727C>T , CM000665.2:g.50342727C>T	GRCh38
NC_000003.11:g.50380158C>T , CM000665.1:g.50380158C>T	GRCh37
NC_000003.10:g.50355162C>T	NCBI36
NG_023270.1:g.3210G>A
NG_042828.1:g.8020G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.701-158G>A MANE Select	ENSP00000231749.3:n.701-158G>A
ENST00000231749.7:c.701-158G>A	ENSP00000231749.3:n.701-158G>A
ENST00000360165.7:c.600-72G>A	ENSP00000353289.3:n.600-72G>A
ENST00000442887.1:c.572-158G>A	ENSP00000393687.1:n.572-158G>A
ENST00000443080.5:c.*453-158G>A	ENSP00000415661.1:n.*453-158G>A
ENST00000475688.1:n.442G>A
NM_001308379.1:c.600-72G>A	NP_001295308.1:n.600-72G>A
NM_015896.2:c.701-158G>A	NP_056980.2:n.701-158G>A
NM_015896.3:c.701-158G>A	NP_056980.2:n.701-158G>A
XM_005265216.2:c.464-158G>A	XP_005265273.1:n.464-158G>A
XM_005265216.3:c.464-158G>A	XP_005265273.1:n.464-158G>A
NM_015896.4:c.701-158G>A MANE Select	NP_056980.2:n.701-158G>A
NM_001308379.2:c.600-72G>A	NP_001295308.1:n.600-72G>A