Canonical Allele Identifier: CA174062391
Gene: NEFL HGNC NCBI

Linked Data

dbSNP Id: rs1006962861
gnomAD v4: 8-24956678-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956678T>C , CM000670.2:g.24956678T>C GRCh38
NC_000008.10:g.24814192T>C , CM000670.1:g.24814192T>C GRCh37
NC_000008.9:g.24870109T>C NCBI36
NG_008492.1:g.4940A>G , LRG_259:g.4940A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-163A>G ENSP00000482169.1:n.-163A>G
ENST00000615973.1:n.44A>G
NM_006158.4:c.-163A>G , LRG_259t1:c.-163A>G NP_006149.2:n.-163A>G