Canonical Allele Identifier: CA401621845
Gene: FN3K HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.801C>G MANE Select ENSP00000300784.7:p.Ile267Met
ENST00000300784.7:c.801C>G ENSP00000300784.7:p.Ile267Met
NM_022158.3:c.801C>G NP_071441.1:p.Ile267Met
XM_024450872.1:c.651C>G XP_024306640.1:p.Ile217Met
NM_022158.4:c.801C>G MANE Select NP_071441.1:p.Ile267Met