Canonical Allele Identifier: CA74634900
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs955969731
gnomAD v3: 3-50345914-A-G
gnomAD v4: 3-50345914-A-G
MyVariant Identifiers: chr3:g.50383345A>G (hg19) chr3:g.50345914A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345914A>G , CM000665.2:g.50345914A>G GRCh38
NC_000003.11:g.50383345A>G , CM000665.1:g.50383345A>G GRCh37
NC_000003.10:g.50358349A>G NCBI36
NG_023270.1:g.23T>C
NG_042828.1:g.4833T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-335T>C ENSP00000231749.3:n.-335T>C
XM_005265216.2:c.-463T>C XP_005265273.1:n.-463T>C
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