Canonical Allele Identifier: CA775764484
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1162078758
MyVariant Identifiers: chr17:g.80685835A>G (hg19) chr17:g.82727959A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727959A>G , CM000679.2:g.82727959A>G GRCh38
NC_000017.10:g.80685835A>G , CM000679.1:g.80685835A>G GRCh37
NC_000017.9:g.78279124A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*788A>G MANE Select ENSP00000269373.6:n.*788A>G
ENST00000269373.10:c.*788A>G ENSP00000269373.6:n.*788A>G
ENST00000571594.1:c.53+792A>G ENSP00000459751.1:n.53+792A>G
NM_024619.3:c.*788A>G NP_078895.2:n.*788A>G
NR_046408.1:n.1896A>G
XM_024450948.1:c.*788A>G XP_024306716.1:n.*788A>G
NM_024619.4:c.*788A>G MANE Select NP_078895.2:n.*788A>G
NR_046408.2:n.1896A>G
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