Canonical Allele Identifier: CA74634717

Gene: ZMYND10

Linked Data

• dbSNP Id: rs888657314
• gnomAD v3: 3-50345764-G-C
• gnomAD v4: 3-50345764-G-C
• MyVariant Identifiers: chr3:g.50383195G>C (hg19) ; chr3:g.50345764G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345764G>C , CM000665.2:g.50345764G>C	GRCh38
NC_000003.11:g.50383195G>C , CM000665.1:g.50383195G>C	GRCh37
NC_000003.10:g.50358199G>C	NCBI36
NG_023270.1:g.173C>G
NG_042828.1:g.4983C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-185C>G	ENSP00000231749.3:n.-185C>G
XM_005265216.2:c.-313C>G	XP_005265273.1:n.-313C>G