Canonical Allele Identifier: CA460021419
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956681-C-G
MyVariant Identifiers: chr8:g.24814195C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956681C>G , CM000670.2:g.24956681C>G GRCh38
NC_000008.10:g.24814195C>G , CM000670.1:g.24814195C>G GRCh37
NC_000008.9:g.24870112C>G NCBI36
NG_008492.1:g.4937G>C , LRG_259:g.4937G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-166G>C ENSP00000482169.1:n.-166G>C
ENST00000615973.1:n.41G>C
NM_006158.4:c.-166G>C , LRG_259t1:c.-166G>C NP_006149.2:n.-166G>C
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