Canonical Allele Identifier: CA1363908913
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703525400
gnomAD v4: 3-50345747-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345747A>G , CM000665.2:g.50345747A>G GRCh38
NC_000003.11:g.50383178A>G , CM000665.1:g.50383178A>G GRCh37
NC_000003.10:g.50358182A>G NCBI36
NG_023270.1:g.190T>C
NG_042828.1:g.5000T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-168T>C ENSP00000231749.3:n.-168T>C
XM_005265216.2:c.-296T>C XP_005265273.1:n.-296T>C
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