Canonical Allele Identifier: CA1047835432
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703525635
gnomAD v3: 3-50345755-C-A
gnomAD v4: 3-50345755-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345755C>A , CM000665.2:g.50345755C>A GRCh38
NC_000003.11:g.50383186C>A , CM000665.1:g.50383186C>A GRCh37
NC_000003.10:g.50358190C>A NCBI36
NG_023270.1:g.182G>T
NG_042828.1:g.4992G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-176G>T ENSP00000231749.3:n.-176G>T
XM_005265216.2:c.-304G>T XP_005265273.1:n.-304G>T
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