Canonical Allele Identifier: CA295269514
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs956231553
gnomAD v3: 17-82727269-T-C
gnomAD v4: 17-82727269-T-C
MyVariant Identifiers: chr17:g.80685145T>C (hg19) chr17:g.82727269T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727269T>C , CM000679.2:g.82727269T>C GRCh38
NC_000017.10:g.80685145T>C , CM000679.1:g.80685145T>C GRCh37
NC_000017.9:g.78278434T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*98T>C MANE Select ENSP00000269373.6:n.*98T>C
ENST00000269373.10:c.*98T>C ENSP00000269373.6:n.*98T>C
ENST00000571594.1:c.53+102T>C ENSP00000459751.1:n.53+102T>C
ENST00000574832.5:c.*985T>C ENSP00000460869.1:n.*985T>C
NM_024619.3:c.*98T>C NP_078895.2:n.*98T>C
NR_046408.1:n.1206T>C
XM_024450948.1:c.*98T>C XP_024306716.1:n.*98T>C
NM_024619.4:c.*98T>C MANE Select NP_078895.2:n.*98T>C
NR_046408.2:n.1206T>C
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