Canonical Allele Identifier: CA2702791487
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs2109361298
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345824A>G , CM000665.2:g.50345824A>G GRCh38
NC_000003.11:g.50383255A>G , CM000665.1:g.50383255A>G GRCh37
NC_000003.10:g.50358259A>G NCBI36
NG_023270.1:g.113T>C
NG_042828.1:g.4923T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-245T>C ENSP00000231749.3:n.-245T>C
XM_005265216.2:c.-373T>C XP_005265273.1:n.-373T>C
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