Canonical Allele Identifier: CA2665848721
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345840-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345840G>T , CM000665.2:g.50345840G>T GRCh38
NC_000003.11:g.50383271G>T , CM000665.1:g.50383271G>T GRCh37
NC_000003.10:g.50358275G>T NCBI36
NG_023270.1:g.97C>A
NG_042828.1:g.4907C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-261C>A ENSP00000231749.3:n.-261C>A
XM_005265216.2:c.-389C>A XP_005265273.1:n.-389C>A
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