Canonical Allele Identifier: CA2665848582
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345751-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345751C>A , CM000665.2:g.50345751C>A GRCh38
NC_000003.11:g.50383182C>A , CM000665.1:g.50383182C>A GRCh37
NC_000003.10:g.50358186C>A NCBI36
NG_023270.1:g.186G>T
NG_042828.1:g.4996G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-172G>T ENSP00000231749.3:n.-172G>T
XM_005265216.2:c.-300G>T XP_005265273.1:n.-300G>T