Canonical Allele Identifier: CA460021837
Gene: NEFL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.24814341T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956827T>C , CM000670.2:g.24956827T>C GRCh38
NC_000008.10:g.24814341T>C , CM000670.1:g.24814341T>C GRCh37
NC_000008.9:g.24870258T>C NCBI36
NG_008492.1:g.4791A>G , LRG_259:g.4791A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-312A>G ENSP00000482169.1:n.-312A>G
NM_006158.4:c.-312A>G , LRG_259t1:c.-312A>G NP_006149.2:n.-312A>G
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