Canonical Allele Identifier: CA8861418
Gene: FN3K HGNC NCBI

Linked Data

dbSNP Id: rs753009394

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750626C>T , CM000679.2:g.82750626C>T GRCh38
NC_000017.10:g.80708502C>T , CM000679.1:g.80708502C>T GRCh37
NC_000017.9:g.78301791C>T NCBI36
NG_011721.1:g.3563C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.801C>T MANE Select ENSP00000300784.7:p.Ile267=
ENST00000300784.7:c.801C>T ENSP00000300784.7:p.Ile267=
NM_022158.3:c.801C>T NP_071441.1:p.Ile267=
XM_024450872.1:c.651C>T XP_024306640.1:p.Ile217=
NM_022158.4:c.801C>T MANE Select NP_071441.1:p.Ile267=