Canonical Allele Identifier: CA460021446
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956691-G-C
MyVariant Identifiers: chr8:g.24814205G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956691G>C , CM000670.2:g.24956691G>C GRCh38
NC_000008.10:g.24814205G>C , CM000670.1:g.24814205G>C GRCh37
NC_000008.9:g.24870122G>C NCBI36
NG_008492.1:g.4927C>G , LRG_259:g.4927C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-176C>G ENSP00000482169.1:n.-176C>G
ENST00000615973.1:n.31C>G
NM_006158.4:c.-176C>G , LRG_259t1:c.-176C>G NP_006149.2:n.-176C>G