Canonical Allele Identifier: CA1047835439
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1292335538
gnomAD v3: 3-50345767-C-G
gnomAD v4: 3-50345767-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345767C>G , CM000665.2:g.50345767C>G GRCh38
NC_000003.11:g.50383198C>G , CM000665.1:g.50383198C>G GRCh37
NC_000003.10:g.50358202C>G NCBI36
NG_023270.1:g.170G>C
NG_042828.1:g.4980G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-188G>C ENSP00000231749.3:n.-188G>C
XM_005265216.2:c.-316G>C XP_005265273.1:n.-316G>C
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