Canonical Allele Identifier: CA74634779
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1022598958
gnomAD v3: 3-50345785-C-T
gnomAD v4: 3-50345785-C-T
MyVariant Identifiers: chr3:g.50383216C>T (hg19) chr3:g.50345785C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345785C>T , CM000665.2:g.50345785C>T GRCh38
NC_000003.11:g.50383216C>T , CM000665.1:g.50383216C>T GRCh37
NC_000003.10:g.50358220C>T NCBI36
NG_023270.1:g.152G>A
NG_042828.1:g.4962G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-206G>A ENSP00000231749.3:n.-206G>A
XM_005265216.2:c.-334G>A XP_005265273.1:n.-334G>A
Search 100 bp 5'
Search 100 bp 3'