Canonical Allele Identifier: CA907892011
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1366127521
gnomAD v3: 3-50345782-C-G
gnomAD v4: 3-50345782-C-G
MyVariant Identifiers: chr3:g.50383213C>G (hg19) chr3:g.50345782C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345782C>G , CM000665.2:g.50345782C>G GRCh38
NC_000003.11:g.50383213C>G , CM000665.1:g.50383213C>G GRCh37
NC_000003.10:g.50358217C>G NCBI36
NG_023270.1:g.155G>C
NG_042828.1:g.4965G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-203G>C ENSP00000231749.3:n.-203G>C
XM_005265216.2:c.-331G>C XP_005265273.1:n.-331G>C
Search 100 bp 5'
Search 100 bp 3'