Canonical Allele Identifier: CA502803459
Gene: FN3K HGNC NCBI

Linked Data

gnomAD v4: 17-82750629-C-G
MyVariant Identifiers: chr17:g.80708505C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750629C>G , CM000679.2:g.82750629C>G GRCh38
NC_000017.10:g.80708505C>G , CM000679.1:g.80708505C>G GRCh37
NC_000017.9:g.78301794C>G NCBI36
NG_011721.1:g.3566C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300784.8:c.804C>G MANE Select ENSP00000300784.7:p.Pro268=
ENST00000300784.7:c.804C>G ENSP00000300784.7:p.Pro268=
NM_022158.3:c.804C>G NP_071441.1:p.Pro268=
XM_024450872.1:c.654C>G XP_024306640.1:p.Pro218=
NM_022158.4:c.804C>G MANE Select NP_071441.1:p.Pro268=
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