Canonical Allele Identifier: CA2665848819
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345897-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345897A>G , CM000665.2:g.50345897A>G GRCh38
NC_000003.11:g.50383328A>G , CM000665.1:g.50383328A>G GRCh37
NC_000003.10:g.50358332A>G NCBI36
NG_023270.1:g.40T>C
NG_042828.1:g.4850T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-318T>C ENSP00000231749.3:n.-318T>C
XM_005265216.2:c.-446T>C XP_005265273.1:n.-446T>C