Canonical Allele Identifier: CA460021659
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956766-C-T
MyVariant Identifiers: chr8:g.24814280C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956766C>T , CM000670.2:g.24956766C>T GRCh38
NC_000008.10:g.24814280C>T , CM000670.1:g.24814280C>T GRCh37
NC_000008.9:g.24870197C>T NCBI36
NG_008492.1:g.4852G>A , LRG_259:g.4852G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-251G>A ENSP00000482169.1:n.-251G>A
NM_006158.4:c.-251G>A , LRG_259t1:c.-251G>A NP_006149.2:n.-251G>A