Canonical Allele Identifier: CA1363908989
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703530082
gnomAD v4: 3-50345867-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345867G>T , CM000665.2:g.50345867G>T GRCh38
NC_000003.11:g.50383298G>T , CM000665.1:g.50383298G>T GRCh37
NC_000003.10:g.50358302G>T NCBI36
NG_023270.1:g.70C>A
NG_042828.1:g.4880C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-288C>A ENSP00000231749.3:n.-288C>A
XM_005265216.2:c.-416C>A XP_005265273.1:n.-416C>A
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