Canonical Allele Identifier: CA502803462
Gene: FN3K HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.80708511T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750635T>A , CM000679.2:g.82750635T>A GRCh38
NC_000017.10:g.80708511T>A , CM000679.1:g.80708511T>A GRCh37
NC_000017.9:g.78301800T>A NCBI36
NG_011721.1:g.3572T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.810T>A MANE Select ENSP00000300784.7:p.Ala270=
ENST00000300784.7:c.810T>A ENSP00000300784.7:p.Ala270=
NM_022158.3:c.810T>A NP_071441.1:p.Ala270=
XM_024450872.1:c.660T>A XP_024306640.1:p.Ala220=
NM_022158.4:c.810T>A MANE Select NP_071441.1:p.Ala270=