Canonical Allele Identifier: CA401621849
Gene: FN3K HGNC NCBI

Linked Data

gnomAD v4: 17-82750628-C-T
MyVariant Identifiers: chr17:g.80708504C>T (hg19) chr17:g.82750628C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750628C>T , CM000679.2:g.82750628C>T GRCh38
NC_000017.10:g.80708504C>T , CM000679.1:g.80708504C>T GRCh37
NC_000017.9:g.78301793C>T NCBI36
NG_011721.1:g.3565C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.803C>T MANE Select ENSP00000300784.7:p.Pro268Leu
ENST00000300784.7:c.803C>T ENSP00000300784.7:p.Pro268Leu
NM_022158.3:c.803C>T NP_071441.1:p.Pro268Leu
XM_024450872.1:c.653C>T XP_024306640.1:p.Pro218Leu
NM_022158.4:c.803C>T MANE Select NP_071441.1:p.Pro268Leu
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