Canonical Allele Identifier: CA1556683338

Gene: F2R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76727626G= , CM000667.2:g.76727626G=	GRCh38
NC_000005.9:g.76023451G= , CM000667.1:g.76023451G=	GRCh37
NC_000005.8:g.76059207G=	NCBI36
NG_032906.1:g.16584G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000319211.5:c.89-4688G= MANE Select	ENSP00000321326.4:n.89-4688G=
ENST00000319211.4:c.89-4688G=	ENSP00000321326.4:n.89-4688G=
NM_001311313.1:c.-397-1086G=	NP_001298242.1:n.-397-1086G=
NM_001992.3:c.89-4688G=	NP_001983.2:n.89-4688G=
NM_001992.4:c.89-4688G=	NP_001983.2:n.89-4688G=
NM_001992.5:c.89-4688G= MANE Select	NP_001983.2:n.89-4688G=
NM_001311313.2:c.-397-1086G=	NP_001298242.1:n.-397-1086G=