Canonical Allele Identifier: CA543053920
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1339893142
gnomAD v2: 3-50383246-G-A
gnomAD v3: 3-50345815-G-A
gnomAD v4: 3-50345815-G-A
MyVariant Identifiers: chr3:g.50383246G>A (hg19) chr3:g.50345815G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345815G>A , CM000665.2:g.50345815G>A GRCh38
NC_000003.11:g.50383246G>A , CM000665.1:g.50383246G>A GRCh37
NC_000003.10:g.50358250G>A NCBI36
NG_023270.1:g.122C>T
NG_042828.1:g.4932C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-236C>T ENSP00000231749.3:n.-236C>T
XM_005265216.2:c.-364C>T XP_005265273.1:n.-364C>T
Search 100 bp 5'
Search 100 bp 3'