Canonical Allele Identifier: CA74634780

Gene: ZMYND10

Linked Data

• dbSNP Id: rs897386236
• gnomAD v3: 3-50345806-G-A
• gnomAD v4: 3-50345806-G-A
• MyVariant Identifiers: chr3:g.50383237G>A (hg19) ; chr3:g.50345806G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345806G>A , CM000665.2:g.50345806G>A	GRCh38
NC_000003.11:g.50383237G>A , CM000665.1:g.50383237G>A	GRCh37
NC_000003.10:g.50358241G>A	NCBI36
NG_023270.1:g.131C>T
NG_042828.1:g.4941C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-227C>T	ENSP00000231749.3:n.-227C>T
XM_005265216.2:c.-355C>T	XP_005265273.1:n.-355C>T