Canonical Allele Identifier: CA295246313
Gene: FN3K HGNC NCBI

Linked Data

dbSNP Id: rs1051611762
gnomAD v2: 17-80708504-C-A
gnomAD v3: 17-82750628-C-A
gnomAD v4: 17-82750628-C-A
MyVariant Identifiers: chr17:g.80708504C>A (hg19) chr17:g.82750628C>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000300784.8:c.803C>A MANE Select ENSP00000300784.7:p.Pro268His
ENST00000300784.7:c.803C>A ENSP00000300784.7:p.Pro268His
NM_022158.3:c.803C>A NP_071441.1:p.Pro268His
XM_024450872.1:c.653C>A XP_024306640.1:p.Pro218His
NM_022158.4:c.803C>A MANE Select NP_071441.1:p.Pro268His
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