Canonical Allele Identifier: CA1363908995

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1703530318

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345874C>G , CM000665.2:g.50345874C>G	GRCh38
NC_000003.11:g.50383305C>G , CM000665.1:g.50383305C>G	GRCh37
NC_000003.10:g.50358309C>G	NCBI36
NG_023270.1:g.63G>C
NG_042828.1:g.4873G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-295G>C	ENSP00000231749.3:n.-295G>C
XM_005265216.2:c.-423G>C	XP_005265273.1:n.-423G>C