Canonical Allele Identifier: CA502803463
Gene: FN3K HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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