Canonical Allele Identifier: CA2665848645
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345790-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345790T>A , CM000665.2:g.50345790T>A GRCh38
NC_000003.11:g.50383221T>A , CM000665.1:g.50383221T>A GRCh37
NC_000003.10:g.50358225T>A NCBI36
NG_023270.1:g.147A>T
NG_042828.1:g.4957A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-211A>T ENSP00000231749.3:n.-211A>T
XM_005265216.2:c.-339A>T XP_005265273.1:n.-339A>T
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