Canonical Allele Identifier: CA907892053
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1396895466
gnomAD v3: 3-50345911-T-C
gnomAD v4: 3-50345911-T-C
MyVariant Identifiers: chr3:g.50383342T>C (hg19) chr3:g.50345911T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345911T>C , CM000665.2:g.50345911T>C GRCh38
NC_000003.11:g.50383342T>C , CM000665.1:g.50383342T>C GRCh37
NC_000003.10:g.50358346T>C NCBI36
NG_023270.1:g.26A>G
NG_042828.1:g.4836A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-332A>G ENSP00000231749.3:n.-332A>G
XM_005265216.2:c.-460A>G XP_005265273.1:n.-460A>G
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