Canonical Allele Identifier: CA907892021
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1399196676
gnomAD v3: 3-50345803-C-T
gnomAD v4: 3-50345803-C-T
MyVariant Identifiers: chr3:g.50383234C>T (hg19) chr3:g.50345803C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345803C>T , CM000665.2:g.50345803C>T GRCh38
NC_000003.11:g.50383234C>T , CM000665.1:g.50383234C>T GRCh37
NC_000003.10:g.50358238C>T NCBI36
NG_023270.1:g.134G>A
NG_042828.1:g.4944G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-224G>A ENSP00000231749.3:n.-224G>A
XM_005265216.2:c.-352G>A XP_005265273.1:n.-352G>A
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