Canonical Allele Identifier: CA1363908927
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs182484324
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345775T>G , CM000665.2:g.50345775T>G GRCh38
NC_000003.11:g.50383206T>G , CM000665.1:g.50383206T>G GRCh37
NC_000003.10:g.50358210T>G NCBI36
NG_023270.1:g.162A>C
NG_042828.1:g.4972A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-196A>C ENSP00000231749.3:n.-196A>C
XM_005265216.2:c.-324A>C XP_005265273.1:n.-324A>C
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