Canonical Allele Identifier: CA1771622571
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956831A= , CM000670.2:g.24956831A= GRCh38
NC_000008.10:g.24814345A= , CM000670.1:g.24814345A= GRCh37
NC_000008.9:g.24870262A= NCBI36
NG_008492.1:g.4787T= , LRG_259:g.4787T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-316T= ENSP00000482169.1:n.-316T=
NM_006158.4:c.-316T= , LRG_259t1:c.-316T= NP_006149.2:n.-316T=