Canonical Allele Identifier: CA322454576

Gene: ZNF280B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.22488645T>C , CM000684.2:g.22488645T>C	GRCh38
NC_000022.10:g.22842970T>C , CM000684.1:g.22842970T>C	GRCh37
NC_000022.9:g.21172970T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_080764.4:c.754A>G MANE Select	NP_542942.2:p.Asn252Asp
ENST00000626650.3:c.754A>G MANE Select	ENSP00000485750.1:p.Asn252Asp
NM_080764.3:c.754A>G	NP_542942.2:p.Asn252Asp
NR_130642.1:n.1530A>G
NR_130642.2:n.1085A>G
NR_130643.1:n.648-2667A>G
NR_130643.2:n.203-2667A>G
ENST00000613655.1:c.754A>G	ENSP00000481008.1:p.Asn252Asp
ENST00000619852.2:c.754A>G	ENSP00000480958.1:p.Asn252Asp
ENST00000626650.2:c.754A>G	ENSP00000485750.1:p.Asn252Asp
XM_011529893.1:c.754A>G	XP_011528195.1:p.Asn252Asp
XM_011529894.1:c.754A>G	XP_011528196.1:p.Asn252Asp
XM_011529895.1:c.754A>G	XP_011528197.1:p.Asn252Asp
XM_011529896.1:c.754A>G	XP_011528198.1:p.Asn252Asp
XM_011529897.1:c.754A>G	XP_011528199.1:p.Asn252Asp
XM_011529897.2:c.754A>G	XP_011528199.1:p.Asn252Asp
XR_002958666.1:n.1569A>G
XR_002958667.1:n.1441A>G
XR_002958668.1:n.1163A>G