Canonical Allele Identifier: CA460021918
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956851-C-A
MyVariant Identifiers: chr8:g.24814365C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956851C>A , CM000670.2:g.24956851C>A GRCh38
NC_000008.10:g.24814365C>A , CM000670.1:g.24814365C>A GRCh37
NC_000008.9:g.24870282C>A NCBI36
NG_008492.1:g.4767G>T , LRG_259:g.4767G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-336G>T ENSP00000482169.1:n.-336G>T
NM_006158.4:c.-336G>T , LRG_259t1:c.-336G>T NP_006149.2:n.-336G>T