Canonical Allele Identifier: CA2665848698
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345817-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345817C>T , CM000665.2:g.50345817C>T GRCh38
NC_000003.11:g.50383248C>T , CM000665.1:g.50383248C>T GRCh37
NC_000003.10:g.50358252C>T NCBI36
NG_023270.1:g.120G>A
NG_042828.1:g.4930G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-238G>A ENSP00000231749.3:n.-238G>A
XM_005265216.2:c.-366G>A XP_005265273.1:n.-366G>A
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