Canonical Allele Identifier: CA174838

Gene: ZNF560

Linked Data

• ClinVar Variation Id: 161815
• ClinVar RCV Id: RCV000149351
• dbSNP Id: rs193920939
• COSMIC: COSM1178716
• MyVariant Identifiers: chr19:g.9578527G>T (hg19) ; chr19:g.9467851G>T (hg38)
• PubMed: PMID:23265383

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9467851G>T , CM000681.2:g.9467851G>T	GRCh38
NC_000019.9:g.9578527G>T , CM000681.1:g.9578527G>T	GRCh37
NC_000019.8:g.9439527G>T	NCBI36
NG_054924.1:g.43842C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301480.5:c.1096C>A MANE Select	ENSP00000301480.3:p.His366Asn
ENST00000301480.4:c.1096C>A	ENSP00000301480.3:p.His366Asn
NM_152476.2:c.1096C>A	NP_689689.2:p.His366Asn
XM_011527696.1:c.1096C>A	XP_011525998.1:p.His366Asn
XM_011527697.1:c.1096C>A	XP_011525999.1:p.His366Asn
XR_936157.1:n.1315C>A
NM_001351678.1:c.778C>A	NP_001338607.1:p.His260Asn
XM_011527696.2:c.1096C>A	XP_011525998.1:p.His366Asn
XM_011527697.2:c.1096C>A	XP_011525999.1:p.His366Asn
XM_017026327.1:c.1096C>A	XP_016881816.1:p.His366Asn
XM_017026328.1:c.1096C>A	XP_016881817.1:p.His366Asn
XM_017026329.1:c.1096C>A	XP_016881818.1:p.His366Asn
XM_017026330.1:c.778C>A	XP_016881819.1:p.His260Asn
XM_024451380.1:c.973C>A	XP_024307148.1:p.His325Asn
NM_001351678.2:c.778C>A	NP_001338607.1:p.His260Asn
NM_152476.3:c.1096C>A MANE Select	NP_689689.2:p.His366Asn