Canonical Allele Identifier: CA2279174114
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs2046849764
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727815G>C , CM000679.2:g.82727815G>C GRCh38
NC_000017.10:g.80685691G>C , CM000679.1:g.80685691G>C GRCh37
NC_000017.9:g.78278980G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*644G>C MANE Select ENSP00000269373.6:n.*644G>C
ENST00000269373.10:c.*644G>C ENSP00000269373.6:n.*644G>C
ENST00000571594.1:c.53+648G>C ENSP00000459751.1:n.53+648G>C
NM_024619.3:c.*644G>C NP_078895.2:n.*644G>C
NR_046408.1:n.1752G>C
XM_024450948.1:c.*644G>C XP_024306716.1:n.*644G>C
NM_024619.4:c.*644G>C MANE Select NP_078895.2:n.*644G>C
NR_046408.2:n.1752G>C
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