Canonical Allele Identifier: CA74631944

Gene: ZMYND10

Linked Data

• dbSNP Id: rs894911754
• MyVariant Identifiers: chr3:g.50380255G>C (hg19) ; chr3:g.50342824G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342824G>C , CM000665.2:g.50342824G>C	GRCh38
NC_000003.11:g.50380255G>C , CM000665.1:g.50380255G>C	GRCh37
NC_000003.10:g.50355259G>C	NCBI36
NG_023270.1:g.3113C>G
NG_042828.1:g.7923C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+94C>G MANE Select	ENSP00000231749.3:n.700+94C>G
ENST00000231749.7:c.700+94C>G	ENSP00000231749.3:n.700+94C>G
ENST00000360165.7:c.600-169C>G	ENSP00000353289.3:n.600-169C>G
ENST00000442887.1:c.571+94C>G	ENSP00000393687.1:n.571+94C>G
ENST00000443080.5:c.*452+94C>G	ENSP00000415661.1:n.*452+94C>G
ENST00000475688.1:n.345C>G
NM_001308379.1:c.600-169C>G	NP_001295308.1:n.600-169C>G
NM_015896.2:c.700+94C>G	NP_056980.2:n.700+94C>G
NM_015896.3:c.700+94C>G	NP_056980.2:n.700+94C>G
XM_005265216.2:c.463+94C>G	XP_005265273.1:n.463+94C>G
XM_005265216.3:c.463+94C>G	XP_005265273.1:n.463+94C>G
NM_015896.4:c.700+94C>G MANE Select	NP_056980.2:n.700+94C>G
NM_001308379.2:c.600-169C>G	NP_001295308.1:n.600-169C>G