Canonical Allele Identifier: CA1363908983

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1703529718

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345850T>C , CM000665.2:g.50345850T>C	GRCh38
NC_000003.11:g.50383281T>C , CM000665.1:g.50383281T>C	GRCh37
NC_000003.10:g.50358285T>C	NCBI36
NG_023270.1:g.87A>G
NG_042828.1:g.4897A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.7:c.-271A>G	ENSP00000231749.3:n.-271A>G
XM_005265216.2:c.-399A>G	XP_005265273.1:n.-399A>G