Canonical Allele Identifier: CA74634731

Gene: ZMYND10

Linked Data

• dbSNP Id: rs111612644
• gnomAD v3: 3-50345774-G-A
• gnomAD v4: 3-50345774-G-A
• MyVariant Identifiers: chr3:g.50383205G>A (hg19) ; chr3:g.50345774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345774G>A , CM000665.2:g.50345774G>A	GRCh38
NC_000003.11:g.50383205G>A , CM000665.1:g.50383205G>A	GRCh37
NC_000003.10:g.50358209G>A	NCBI36
NG_023270.1:g.163C>T
NG_042828.1:g.4973C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-195C>T	ENSP00000231749.3:n.-195C>T
XM_005265216.2:c.-323C>T	XP_005265273.1:n.-323C>T