Canonical Allele Identifier: CA14391363
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1046896

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727657C>T , CM000679.2:g.82727657C>T GRCh38
NC_000017.10:g.80685533C>T , CM000679.1:g.80685533C>T GRCh37
NC_000017.9:g.78278822C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000269373.10:c.*486C>T ENSP00000269373.6:p.=
ENST00000571594.1:n.53+490C>T ENSP00000459751.1:p.=
NM_024619.3:c.*486C>T NP_078895.2:p.=
XM_024450948.1:c.*486C>T XP_024306716.1:p.=
NM_024619.4:c.*486C>T MANE Select NP_078895.2:p.=