Canonical Allele Identifier: CA2321543498
Gene: NFILZ HGNC NCBI

Linked Data

dbSNP Id: rs781607401
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8679500C>A , CM000681.2:g.8679500C>A GRCh38
NC_000019.9:g.8789764C>A , CM000681.1:g.8789764C>A GRCh37
NC_000019.8:g.8650764C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000570582.4:c.*1865C>A ENSP00000500121.1:n.*1865C>A
ENST00000671902.2:c.*1865C>A ENSP00000500604.1:n.*1865C>A
ENST00000673603.2:c.*1865C>A ENSP00000499970.1:n.*1865C>A
ENST00000691075.1:c.*1865C>A MANE Select ENSP00000509575.1:n.*1865C>A
NM_001378599.1:c.*1865C>A NP_001365528.1:n.*1865C>A
NM_001378600.1:c.*1865C>A MANE Select NP_001365529.1:n.*1865C>A
NM_001378601.1:c.*1865C>A NP_001365530.1:n.*1865C>A
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