Canonical Allele Identifier: CA2397314297
Gene: ZNF280B HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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