Canonical Allele Identifier: CA918222145
Gene: NEFL HGNC NCBI

Linked Data

dbSNP Id: rs1586129526

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956785dup , CM000670.2:g.24956785dup GRCh38
NC_000008.10:g.24814299dup , CM000670.1:g.24814299dup GRCh37
NC_000008.9:g.24870216dup NCBI36
NG_008492.1:g.4833dup , LRG_259:g.4833dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-270dup ENSP00000482169.1:n.-270dup
NM_006158.4:c.-270dup , LRG_259t1:c.-270dup NP_006149.2:n.-270dup