Canonical Allele Identifier: CA2640698028
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v4: 17-82727639-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727639A>G , CM000679.2:g.82727639A>G GRCh38
NC_000017.10:g.80685515A>G , CM000679.1:g.80685515A>G GRCh37
NC_000017.9:g.78278804A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*468A>G MANE Select ENSP00000269373.6:n.*468A>G
ENST00000269373.10:c.*468A>G ENSP00000269373.6:n.*468A>G
ENST00000571594.1:c.53+472A>G ENSP00000459751.1:n.53+472A>G
NM_024619.3:c.*468A>G NP_078895.2:n.*468A>G
NR_046408.1:n.1576A>G
XM_024450948.1:c.*468A>G XP_024306716.1:n.*468A>G
NM_024619.4:c.*468A>G MANE Select NP_078895.2:n.*468A>G
NR_046408.2:n.1576A>G
Search 100 bp 5'
Search 100 bp 3'