Canonical Allele Identifier: CA401621857
Gene: FN3K HGNC NCBI

Linked Data

dbSNP Id: rs2047009311
MyVariant Identifiers: chr17:g.80708508G>C (hg19) chr17:g.82750632G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750632G>C , CM000679.2:g.82750632G>C GRCh38
NC_000017.10:g.80708508G>C , CM000679.1:g.80708508G>C GRCh37
NC_000017.9:g.78301797G>C NCBI36
NG_011721.1:g.3569G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.807G>C MANE Select ENSP00000300784.7:p.Lys269Asn
ENST00000300784.7:c.807G>C ENSP00000300784.7:p.Lys269Asn
NM_022158.3:c.807G>C NP_071441.1:p.Lys269Asn
XM_024450872.1:c.657G>C XP_024306640.1:p.Lys219Asn
NM_022158.4:c.807G>C MANE Select NP_071441.1:p.Lys269Asn
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