Canonical Allele Identifier: CA1363908978
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs1703529389
gnomAD v4: 3-50345840-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345840G>A , CM000665.2:g.50345840G>A GRCh38
NC_000003.11:g.50383271G>A , CM000665.1:g.50383271G>A GRCh37
NC_000003.10:g.50358275G>A NCBI36
NG_023270.1:g.97C>T
NG_042828.1:g.4907C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.7:c.-261C>T ENSP00000231749.3:n.-261C>T
XM_005265216.2:c.-389C>T XP_005265273.1:n.-389C>T
Search 100 bp 5'
Search 100 bp 3'