Canonical Allele Identifier: CA322456248

Gene: ZNF280B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.22490916C>T , CM000684.2:g.22490916C>T	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000626650.3:c.-68-1450G>A MANE Select	ENSP00000485750.1:n.-68-1450G>A
ENST00000619852.2:c.-68-1450G>A	ENSP00000480958.1:n.-68-1450G>A
ENST00000626650.2:c.-68-1450G>A	ENSP00000485750.1:n.-68-1450G>A
NM_080764.3:c.-68-1450G>A	NP_542942.2:n.-68-1450G>A
NR_130642.1:n.709-1450G>A
NR_130643.1:n.647+3147G>A
XM_011529893.1:c.-68-1450G>A	XP_011528195.1:n.-68-1450G>A
XM_011529894.1:c.-68-1450G>A	XP_011528196.1:n.-68-1450G>A
XM_011529895.1:c.-68-1450G>A	XP_011528197.1:n.-68-1450G>A
XM_011529896.1:c.-68-1450G>A	XP_011528198.1:n.-68-1450G>A
XM_011529897.1:c.-68-1450G>A	XP_011528199.1:n.-68-1450G>A
XM_011529897.2:c.-68-1450G>A	XP_011528199.1:n.-68-1450G>A
XR_002958666.1:n.748-1450G>A
XR_002958667.1:n.620-1450G>A
XR_002958668.1:n.342-1450G>A
NM_080764.4:c.-68-1450G>A MANE Select	NP_542942.2:n.-68-1450G>A
NR_130642.2:n.264-1450G>A
NR_130643.2:n.202+3147G>A