Canonical Allele Identifier: CA8861421
Gene: FN3K HGNC NCBI

Linked Data

dbSNP Id: rs750001644
ExAC: 17:80708514 G / A
gnomAD v2: 17-80708514-G-A
gnomAD v4: 17-82750638-G-A
MyVariant Identifiers: chr17:g.80708514G>A (hg19) chr17:g.82750638G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750638G>A , CM000679.2:g.82750638G>A GRCh38
NC_000017.10:g.80708514G>A , CM000679.1:g.80708514G>A GRCh37
NC_000017.9:g.78301803G>A NCBI36
NG_011721.1:g.3575G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.813G>A MANE Select ENSP00000300784.7:p.Pro271=
ENST00000300784.7:c.813G>A ENSP00000300784.7:p.Pro271=
NM_022158.3:c.813G>A NP_071441.1:p.Pro271=
XM_024450872.1:c.663G>A XP_024306640.1:p.Pro221=
NM_022158.4:c.813G>A MANE Select NP_071441.1:p.Pro271=
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