Canonical Allele Identifier: CA8861420
Gene: FN3K HGNC NCBI

Linked Data

dbSNP Id: rs764480267

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750637C>T , CM000679.2:g.82750637C>T GRCh38
NC_000017.10:g.80708513C>T , CM000679.1:g.80708513C>T GRCh37
NC_000017.9:g.78301802C>T NCBI36
NG_011721.1:g.3574C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.812C>T MANE Select ENSP00000300784.7:p.Pro271Leu
ENST00000300784.7:c.812C>T ENSP00000300784.7:p.Pro271Leu
NM_022158.3:c.812C>T NP_071441.1:p.Pro271Leu
XM_024450872.1:c.662C>T XP_024306640.1:p.Pro221Leu
NM_022158.4:c.812C>T MANE Select NP_071441.1:p.Pro271Leu