Canonical Allele Identifier: CA2686596940
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956795-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956798del , CM000670.2:g.24956798del GRCh38
NC_000008.10:g.24814312del , CM000670.1:g.24814312del GRCh37
NC_000008.9:g.24870229del NCBI36
NG_008492.1:g.4822del , LRG_259:g.4822del

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-281del ENSP00000482169.1:n.-281del
NM_006158.4:c.-281del , LRG_259t1:c.-281del NP_006149.2:n.-281del
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