Canonical Allele Identifier: CA2581327351
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82728014C>A , CM000679.2:g.82728014C>A GRCh38
NC_000017.10:g.80685890C>A , CM000679.1:g.80685890C>A GRCh37
NC_000017.9:g.78279179C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.10:c.*843C>A ENSP00000269373.6:n.*843C>A
ENST00000571594.1:c.53+847C>A ENSP00000459751.1:n.53+847C>A
XM_024450948.1:c.*843C>A XP_024306716.1:n.*843C>A