Canonical Allele Identifier: CA401621864
Gene: FN3K HGNC NCBI

Linked Data

gnomAD v4: 17-82750634-C-T
MyVariant Identifiers: chr17:g.80708510C>T (hg19) chr17:g.82750634C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750634C>T , CM000679.2:g.82750634C>T GRCh38
NC_000017.10:g.80708510C>T , CM000679.1:g.80708510C>T GRCh37
NC_000017.9:g.78301799C>T NCBI36
NG_011721.1:g.3571C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000300784.8:c.809C>T MANE Select ENSP00000300784.7:p.Ala270Val
ENST00000300784.7:c.809C>T ENSP00000300784.7:p.Ala270Val
NM_022158.3:c.809C>T NP_071441.1:p.Ala270Val
XM_024450872.1:c.659C>T XP_024306640.1:p.Ala220Val
NM_022158.4:c.809C>T MANE Select NP_071441.1:p.Ala270Val
Search 100 bp 5'
Search 100 bp 3'