Canonical Allele Identifier: CA1047835463
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703529971
gnomAD v3: 3-50345864-C-A
gnomAD v4: 3-50345864-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345864C>A , CM000665.2:g.50345864C>A GRCh38
NC_000003.11:g.50383295C>A , CM000665.1:g.50383295C>A GRCh37
NC_000003.10:g.50358299C>A NCBI36
NG_023270.1:g.73G>T
NG_042828.1:g.4883G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-285G>T ENSP00000231749.3:n.-285G>T
XM_005265216.2:c.-413G>T XP_005265273.1:n.-413G>T