Canonical Allele Identifier: CA460021399
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956674-T-C
MyVariant Identifiers: chr8:g.24814188T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956674T>C , CM000670.2:g.24956674T>C GRCh38
NC_000008.10:g.24814188T>C , CM000670.1:g.24814188T>C GRCh37
NC_000008.9:g.24870105T>C NCBI36
NG_008492.1:g.4944A>G , LRG_259:g.4944A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-159A>G ENSP00000482169.1:n.-159A>G
ENST00000615973.1:n.48A>G
NM_006158.4:c.-159A>G , LRG_259t1:c.-159A>G NP_006149.2:n.-159A>G
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