Canonical Allele Identifier: CA401621868
Gene: FN3K HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.80708513C>G (hg19) chr17:g.82750637C>G (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000300784.8:c.812C>G MANE Select ENSP00000300784.7:p.Pro271Arg
ENST00000300784.7:c.812C>G ENSP00000300784.7:p.Pro271Arg
NM_022158.3:c.812C>G NP_071441.1:p.Pro271Arg
XM_024450872.1:c.662C>G XP_024306640.1:p.Pro221Arg
NM_022158.4:c.812C>G MANE Select NP_071441.1:p.Pro271Arg
Search 100 bp 5'
Search 100 bp 3'