Canonical Allele Identifier: CA2279173839
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs2243446

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727250T>A , CM000679.2:g.82727250T>A GRCh38
NC_000017.10:g.80685126T>A , CM000679.1:g.80685126T>A GRCh37
NC_000017.9:g.78278415T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*79T>A MANE Select ENSP00000269373.6:n.*79T>A
ENST00000269373.10:c.*79T>A ENSP00000269373.6:n.*79T>A
ENST00000571594.1:c.53+83T>A ENSP00000459751.1:n.53+83T>A
ENST00000574832.5:c.*966T>A ENSP00000460869.1:n.*966T>A
XM_024450948.1:c.*79T>A XP_024306716.1:n.*79T>A
NM_024619.4:c.*79T>A MANE Select NP_078895.2:n.*79T>A
NR_046408.2:n.1187T>A