Canonical Allele Identifier: CA2518647990
Gene: F2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76727584_76727586del , CM000667.2:g.76727584_76727586del GRCh38
NC_000005.9:g.76023409_76023411del , CM000667.1:g.76023409_76023411del GRCh37
NC_000005.8:g.76059165_76059167del NCBI36
NG_032906.1:g.16542_16544del

Transcript Alleles

HGVS Amino-acid change
ENST00000319211.5:c.89-4730_89-4728del MANE Select ENSP00000321326.4:n.89-4730_89-4728del
ENST00000319211.4:c.89-4730_89-4728del ENSP00000321326.4:n.89-4730_89-4728del
NM_001311313.1:c.-397-1128_-397-1126del NP_001298242.1:n.-397-1128_-397-1126del
NM_001992.3:c.89-4730_89-4728del NP_001983.2:n.89-4730_89-4728del
NM_001992.4:c.89-4730_89-4728del NP_001983.2:n.89-4730_89-4728del
NM_001992.5:c.89-4730_89-4728del MANE Select NP_001983.2:n.89-4730_89-4728del
NM_001311313.2:c.-397-1128_-397-1126del NP_001298242.1:n.-397-1128_-397-1126del
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