Canonical Allele Identifier: CA1556683302

Gene: F2R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76727577C= , CM000667.2:g.76727577C=	GRCh38
NC_000005.9:g.76023402C= , CM000667.1:g.76023402C=	GRCh37
NC_000005.8:g.76059158C=	NCBI36
NG_032906.1:g.16535C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000319211.5:c.89-4737C= MANE Select	ENSP00000321326.4:n.89-4737C=
ENST00000319211.4:c.89-4737C=	ENSP00000321326.4:n.89-4737C=
NM_001311313.1:c.-397-1135C=	NP_001298242.1:n.-397-1135C=
NM_001992.3:c.89-4737C=	NP_001983.2:n.89-4737C=
NM_001992.4:c.89-4737C=	NP_001983.2:n.89-4737C=
NM_001992.5:c.89-4737C= MANE Select	NP_001983.2:n.89-4737C=
NM_001311313.2:c.-397-1135C=	NP_001298242.1:n.-397-1135C=