Canonical Allele Identifier: CA15638578
Gene: NEBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21278636C>A , CM000672.2:g.21278636C>A GRCh38
NC_000010.10:g.21567565C>A , CM000672.1:g.21567565C>A GRCh37
NC_000010.9:g.21607571C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000675702.1:n.182+14194G>T
NM_001377326.1:c.-40+14194G>T NP_001364255.1:n.-40+14194G>T
NM_001377327.1:c.-206+14194G>T NP_001364256.1:n.-206+14194G>T