Canonical Allele Identifier: CA401621842
Gene: FN3K HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.80708501T>A (hg19) chr17:g.82750625T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750625T>A , CM000679.2:g.82750625T>A GRCh38
NC_000017.10:g.80708501T>A , CM000679.1:g.80708501T>A GRCh37
NC_000017.9:g.78301790T>A NCBI36
NG_011721.1:g.3562T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.800T>A MANE Select ENSP00000300784.7:p.Ile267Asn
ENST00000300784.7:c.800T>A ENSP00000300784.7:p.Ile267Asn
NM_022158.3:c.800T>A NP_071441.1:p.Ile267Asn
XM_024450872.1:c.650T>A XP_024306640.1:p.Ile217Asn
NM_022158.4:c.800T>A MANE Select NP_071441.1:p.Ile267Asn
Search 100 bp 5'
Search 100 bp 3'