Canonical Allele Identifier: CA502803461
Gene: FN3K HGNC NCBI

Linked Data

gnomAD v4: 17-82750632-G-A
MyVariant Identifiers: chr17:g.80708508G>A (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000300784.8:c.807G>A MANE Select ENSP00000300784.7:p.Lys269=
ENST00000300784.7:c.807G>A ENSP00000300784.7:p.Lys269=
NM_022158.3:c.807G>A NP_071441.1:p.Lys269=
XM_024450872.1:c.657G>A XP_024306640.1:p.Lys219=
NM_022158.4:c.807G>A MANE Select NP_071441.1:p.Lys269=
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