Canonical Allele Identifier: CA2665848667
Gene: ZMYND10 HGNC NCBI

Linked Data

gnomAD v4: 3-50345798-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345798G>A , CM000665.2:g.50345798G>A GRCh38
NC_000003.11:g.50383229G>A , CM000665.1:g.50383229G>A GRCh37
NC_000003.10:g.50358233G>A NCBI36
NG_023270.1:g.139C>T
NG_042828.1:g.4949C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-219C>T ENSP00000231749.3:n.-219C>T
XM_005265216.2:c.-347C>T XP_005265273.1:n.-347C>T