Canonical Allele Identifier: CA2665848634
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345783-G-C

Genomic Alleles

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

Transcript Alleles

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