Canonical Allele Identifier: CA1047835426
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703525578
gnomAD v3: 3-50345750-G-A
gnomAD v4: 3-50345750-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345750G>A , CM000665.2:g.50345750G>A GRCh38
NC_000003.11:g.50383181G>A , CM000665.1:g.50383181G>A GRCh37
NC_000003.10:g.50358185G>A NCBI36
NG_023270.1:g.187C>T
NG_042828.1:g.4997C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-171C>T ENSP00000231749.3:n.-171C>T
XM_005265216.2:c.-299C>T XP_005265273.1:n.-299C>T