Canonical Allele Identifier: CA2321543492
Gene: NFILZ HGNC NCBI

Linked Data

dbSNP Id: rs2043135407
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8679479T>C , CM000681.2:g.8679479T>C GRCh38
NC_000019.9:g.8789743T>C , CM000681.1:g.8789743T>C GRCh37
NC_000019.8:g.8650743T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000570582.4:c.*1844T>C ENSP00000500121.1:n.*1844T>C
ENST00000671902.2:c.*1844T>C ENSP00000500604.1:n.*1844T>C
ENST00000673603.2:c.*1844T>C ENSP00000499970.1:n.*1844T>C
ENST00000691075.1:c.*1844T>C MANE Select ENSP00000509575.1:n.*1844T>C
NM_001378599.1:c.*1844T>C NP_001365528.1:n.*1844T>C
NM_001378600.1:c.*1844T>C MANE Select NP_001365529.1:n.*1844T>C
NM_001378601.1:c.*1844T>C NP_001365530.1:n.*1844T>C
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