Canonical Allele Identifier: CA460021755
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956799-G-T
MyVariant Identifiers: chr8:g.24814313G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956799G>T , CM000670.2:g.24956799G>T GRCh38
NC_000008.10:g.24814313G>T , CM000670.1:g.24814313G>T GRCh37
NC_000008.9:g.24870230G>T NCBI36
NG_008492.1:g.4819C>A , LRG_259:g.4819C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-284C>A ENSP00000482169.1:n.-284C>A
NM_006158.4:c.-284C>A , LRG_259t1:c.-284C>A NP_006149.2:n.-284C>A