Canonical Allele Identifier: CA460019967
Gene: NEFL HGNC NCBI

Linked Data

dbSNP Id: rs760359146
gnomAD v3: 8-24952660-T-G
gnomAD v4: 8-24952660-T-G
MyVariant Identifiers: chr8:g.24810173T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24952660T>G , CM000670.2:g.24952660T>G GRCh38
NC_000008.10:g.24810173T>G , CM000670.1:g.24810173T>G GRCh37
NC_000008.9:g.24866090T>G NCBI36
NG_008492.1:g.8958A>C , LRG_259:g.8958A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000610854.2:c.*150A>C MANE Select ENSP00000482169.2:n.*150A>C
ENST00000610854.1:c.*150A>C ENSP00000482169.1:n.*150A>C
ENST00000619417.1:c.*647A>C ENSP00000483690.1:n.*647A>C
NM_006158.4:c.*150A>C , LRG_259t1:c.*150A>C NP_006149.2:n.*150A>C
NM_006158.5:c.*150A>C MANE Select NP_006149.2:n.*150A>C
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