Canonical Allele Identifier: CA74634743

Gene: ZMYND10

Linked Data

• dbSNP Id: rs182484324
• gnomAD v2: 3-50383206-T-A
• gnomAD v3: 3-50345775-T-A
• gnomAD v4: 3-50345775-T-A
• MyVariant Identifiers: chr3:g.50383206T>A (hg19) ; chr3:g.50345775T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345775T>A , CM000665.2:g.50345775T>A	GRCh38
NC_000003.11:g.50383206T>A , CM000665.1:g.50383206T>A	GRCh37
NC_000003.10:g.50358210T>A	NCBI36
NG_023270.1:g.162A>T
NG_042828.1:g.4972A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-196A>T	ENSP00000231749.3:n.-196A>T
XM_005265216.2:c.-324A>T	XP_005265273.1:n.-324A>T