Canonical Allele Identifier: CA460021232
Gene: NEFL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.24814129C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956615C>A , CM000670.2:g.24956615C>A GRCh38
NC_000008.10:g.24814129C>A , CM000670.1:g.24814129C>A GRCh37
NC_000008.9:g.24870046C>A NCBI36
NG_008492.1:g.5003G>T , LRG_259:g.5003G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-100G>T ENSP00000482169.1:n.-100G>T
ENST00000615973.1:n.107G>T
NM_006158.4:c.-100G>T , LRG_259t1:c.-100G>T NP_006149.2:n.-100G>T
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