Canonical Allele Identifier: CA2597268165
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs2109361181
gnomAD v3: 3-50345752-G-A
gnomAD v4: 3-50345752-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345752G>A , CM000665.2:g.50345752G>A GRCh38
NC_000003.11:g.50383183G>A , CM000665.1:g.50383183G>A GRCh37
NC_000003.10:g.50358187G>A NCBI36
NG_023270.1:g.185C>T
NG_042828.1:g.4995C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-173C>T ENSP00000231749.3:n.-173C>T
XM_005265216.2:c.-301C>T XP_005265273.1:n.-301C>T