Canonical Allele Identifier: CA460021441
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956689-C-G
MyVariant Identifiers: chr8:g.24814203C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956689C>G , CM000670.2:g.24956689C>G GRCh38
NC_000008.10:g.24814203C>G , CM000670.1:g.24814203C>G GRCh37
NC_000008.9:g.24870120C>G NCBI36
NG_008492.1:g.4929G>C , LRG_259:g.4929G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-174G>C ENSP00000482169.1:n.-174G>C
ENST00000615973.1:n.33G>C
NM_006158.4:c.-174G>C , LRG_259t1:c.-174G>C NP_006149.2:n.-174G>C