Canonical Allele Identifier: CA775764417
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1183729739
MyVariant Identifiers: chr17:g.80685746T>C (hg19) chr17:g.82727870T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727870T>C , CM000679.2:g.82727870T>C GRCh38
NC_000017.10:g.80685746T>C , CM000679.1:g.80685746T>C GRCh37
NC_000017.9:g.78279035T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*699T>C MANE Select ENSP00000269373.6:n.*699T>C
ENST00000269373.10:c.*699T>C ENSP00000269373.6:n.*699T>C
ENST00000571594.1:c.53+703T>C ENSP00000459751.1:n.53+703T>C
NM_024619.3:c.*699T>C NP_078895.2:n.*699T>C
NR_046408.1:n.1807T>C
XM_024450948.1:c.*699T>C XP_024306716.1:n.*699T>C
NM_024619.4:c.*699T>C MANE Select NP_078895.2:n.*699T>C
NR_046408.2:n.1807T>C
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