Canonical Allele Identifier: CA174062397
Gene: NEFL HGNC NCBI

Linked Data

dbSNP Id: rs1018299976
gnomAD v4: 8-24956682-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956682G>A , CM000670.2:g.24956682G>A GRCh38
NC_000008.10:g.24814196G>A , CM000670.1:g.24814196G>A GRCh37
NC_000008.9:g.24870113G>A NCBI36
NG_008492.1:g.4936C>T , LRG_259:g.4936C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-167C>T ENSP00000482169.1:n.-167C>T
ENST00000615973.1:n.40C>T
NM_006158.4:c.-167C>T , LRG_259t1:c.-167C>T NP_006149.2:n.-167C>T