Canonical Allele Identifier: CA460021229
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956614-G-T
MyVariant Identifiers: chr8:g.24814128G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956614G>T , CM000670.2:g.24956614G>T GRCh38
NC_000008.10:g.24814128G>T , CM000670.1:g.24814128G>T GRCh37
NC_000008.9:g.24870045G>T NCBI36
NG_008492.1:g.5004C>A , LRG_259:g.5004C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-99C>A ENSP00000482169.1:n.-99C>A
ENST00000615973.1:n.108C>A
NM_006158.4:c.-99C>A , LRG_259t1:c.-99C>A NP_006149.2:n.-99C>A
Search 100 bp 5'
Search 100 bp 3'