Canonical Allele Identifier: CA502803453
Gene: FN3K HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.80708502C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750626C>A , CM000679.2:g.82750626C>A GRCh38
NC_000017.10:g.80708502C>A , CM000679.1:g.80708502C>A GRCh37
NC_000017.9:g.78301791C>A NCBI36
NG_011721.1:g.3563C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000300784.8:c.801C>A MANE Select ENSP00000300784.7:p.Ile267=
ENST00000300784.7:c.801C>A ENSP00000300784.7:p.Ile267=
NM_022158.3:c.801C>A NP_071441.1:p.Ile267=
XM_024450872.1:c.651C>A XP_024306640.1:p.Ile217=
NM_022158.4:c.801C>A MANE Select NP_071441.1:p.Ile267=
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