Canonical Allele Identifier: CA907892007

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1366127521
• gnomAD v3: 3-50345782-C-A
• gnomAD v4: 3-50345782-C-A
• MyVariant Identifiers: chr3:g.50383213C>A (hg19) ; chr3:g.50345782C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345782C>A , CM000665.2:g.50345782C>A	GRCh38
NC_000003.11:g.50383213C>A , CM000665.1:g.50383213C>A	GRCh37
NC_000003.10:g.50358217C>A	NCBI36
NG_023270.1:g.155G>T
NG_042828.1:g.4965G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-203G>T	ENSP00000231749.3:n.-203G>T
XM_005265216.2:c.-331G>T	XP_005265273.1:n.-331G>T