Canonical Allele Identifier: CA460021838
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956827-T-G
MyVariant Identifiers: chr8:g.24814341T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956827T>G , CM000670.2:g.24956827T>G GRCh38
NC_000008.10:g.24814341T>G , CM000670.1:g.24814341T>G GRCh37
NC_000008.9:g.24870258T>G NCBI36
NG_008492.1:g.4791A>C , LRG_259:g.4791A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-312A>C ENSP00000482169.1:n.-312A>C
NM_006158.4:c.-312A>C , LRG_259t1:c.-312A>C NP_006149.2:n.-312A>C