Canonical Allele Identifier: CA1363908907
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703525215
gnomAD v4: 3-50345739-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345739G>A , CM000665.2:g.50345739G>A GRCh38
NC_000003.11:g.50383170G>A , CM000665.1:g.50383170G>A GRCh37
NC_000003.10:g.50358174G>A NCBI36
NG_023270.1:g.198C>T
NG_042828.1:g.5008C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-160C>T ENSP00000231749.3:n.-160C>T
NM_001308379.1:c.-160C>T NP_001295308.1:n.-160C>T
NM_015896.3:c.-160C>T NP_056980.2:n.-160C>T
XM_005265216.2:c.-288C>T XP_005265273.1:n.-288C>T