Canonical Allele Identifier: CA1363908944
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1276344799
gnomAD v4: 3-50345796-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345796C>T , CM000665.2:g.50345796C>T GRCh38
NC_000003.11:g.50383227C>T , CM000665.1:g.50383227C>T GRCh37
NC_000003.10:g.50358231C>T NCBI36
NG_023270.1:g.141G>A
NG_042828.1:g.4951G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-217G>A ENSP00000231749.3:n.-217G>A
XM_005265216.2:c.-345G>A XP_005265273.1:n.-345G>A