Canonical Allele Identifier: CA2543792032
Gene: F2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76727578_76727579del , CM000667.2:g.76727578_76727579del GRCh38
NC_000005.9:g.76023403_76023404del , CM000667.1:g.76023403_76023404del GRCh37
NC_000005.8:g.76059159_76059160del NCBI36
NG_032906.1:g.16536_16537del

Transcript Alleles

HGVS Amino-acid change
ENST00000319211.5:c.89-4736_89-4735del MANE Select ENSP00000321326.4:n.89-4736_89-4735del
ENST00000319211.4:c.89-4736_89-4735del ENSP00000321326.4:n.89-4736_89-4735del
NM_001311313.1:c.-397-1134_-397-1133del NP_001298242.1:n.-397-1134_-397-1133del
NM_001992.3:c.89-4736_89-4735del NP_001983.2:n.89-4736_89-4735del
NM_001992.4:c.89-4736_89-4735del NP_001983.2:n.89-4736_89-4735del
NM_001992.5:c.89-4736_89-4735del MANE Select NP_001983.2:n.89-4736_89-4735del
NM_001311313.2:c.-397-1134_-397-1133del NP_001298242.1:n.-397-1134_-397-1133del
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