Canonical Allele Identifier: CA401621854
Gene: FN3K HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.80708507A>C (hg19) chr17:g.82750631A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750631A>C , CM000679.2:g.82750631A>C GRCh38
NC_000017.10:g.80708507A>C , CM000679.1:g.80708507A>C GRCh37
NC_000017.9:g.78301796A>C NCBI36
NG_011721.1:g.3568A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000300784.8:c.806A>C MANE Select ENSP00000300784.7:p.Lys269Thr
ENST00000300784.7:c.806A>C ENSP00000300784.7:p.Lys269Thr
NM_022158.3:c.806A>C NP_071441.1:p.Lys269Thr
XM_024450872.1:c.656A>C XP_024306640.1:p.Lys219Thr
NM_022158.4:c.806A>C MANE Select NP_071441.1:p.Lys269Thr
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