Canonical Allele Identifier: CA884359095
Gene: NFILZ HGNC NCBI

Linked Data

dbSNP Id: rs1277912110
MyVariant Identifiers: chr19:g.8679477G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8679477G>A , CM000681.2:g.8679477G>A GRCh38
NC_000019.9:g.8789741G>A , CM000681.1:g.8789741G>A GRCh37
NC_000019.8:g.8650741G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000570582.4:c.*1842G>A ENSP00000500121.1:n.*1842G>A
ENST00000671902.2:c.*1842G>A ENSP00000500604.1:n.*1842G>A
ENST00000673603.2:c.*1842G>A ENSP00000499970.1:n.*1842G>A
ENST00000691075.1:c.*1842G>A MANE Select ENSP00000509575.1:n.*1842G>A
NM_001378599.1:c.*1842G>A NP_001365528.1:n.*1842G>A
NM_001378600.1:c.*1842G>A MANE Select NP_001365529.1:n.*1842G>A
NM_001378601.1:c.*1842G>A NP_001365530.1:n.*1842G>A
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