Canonical Allele Identifier: CA1771622565
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956826A= , CM000670.2:g.24956826A= GRCh38
NC_000008.10:g.24814340A= , CM000670.1:g.24814340A= GRCh37
NC_000008.9:g.24870257A= NCBI36
NG_008492.1:g.4792T= , LRG_259:g.4792T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-311T= ENSP00000482169.1:n.-311T=
NM_006158.4:c.-311T= , LRG_259t1:c.-311T= NP_006149.2:n.-311T=