Canonical Allele Identifier: CA460021378
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956667-C-A
MyVariant Identifiers: chr8:g.24814181C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956667C>A , CM000670.2:g.24956667C>A GRCh38
NC_000008.10:g.24814181C>A , CM000670.1:g.24814181C>A GRCh37
NC_000008.9:g.24870098C>A NCBI36
NG_008492.1:g.4951G>T , LRG_259:g.4951G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-152G>T ENSP00000482169.1:n.-152G>T
ENST00000615973.1:n.55G>T
NM_006158.4:c.-152G>T , LRG_259t1:c.-152G>T NP_006149.2:n.-152G>T