Canonical Allele Identifier: CA74634755
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs587765656
gnomAD v2: 3-50383214-G-A
gnomAD v3: 3-50345783-G-A
gnomAD v4: 3-50345783-G-A
MyVariant Identifiers: chr3:g.50383214G>A (hg19) chr3:g.50345783G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345783G>A , CM000665.2:g.50345783G>A GRCh38
NC_000003.11:g.50383214G>A , CM000665.1:g.50383214G>A GRCh37
NC_000003.10:g.50358218G>A NCBI36
NG_023270.1:g.154C>T
NG_042828.1:g.4964C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-204C>T ENSP00000231749.3:n.-204C>T
XM_005265216.2:c.-332C>T XP_005265273.1:n.-332C>T
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