Canonical Allele Identifier: CA460021431
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956685-A-T
MyVariant Identifiers: chr8:g.24814199A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956685A>T , CM000670.2:g.24956685A>T GRCh38
NC_000008.10:g.24814199A>T , CM000670.1:g.24814199A>T GRCh37
NC_000008.9:g.24870116A>T NCBI36
NG_008492.1:g.4933T>A , LRG_259:g.4933T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-170T>A ENSP00000482169.1:n.-170T>A
ENST00000615973.1:n.37T>A
NM_006158.4:c.-170T>A , LRG_259t1:c.-170T>A NP_006149.2:n.-170T>A
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