Canonical Allele Identifier: CA1969072228

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726098G= , CM000673.2:g.46726098G=	GRCh38
NC_000011.9:g.46747648G= , CM000673.1:g.46747648G=	GRCh37
NC_000011.8:g.46704224G=	NCBI36
NG_008953.1:g.11906G= , LRG_551:g.11906G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.799G= MANE Select	ENSP00000308541.5:p.Gly267=
ENST00000311907.9:c.799G=	ENSP00000308541.5:p.Gly267=
ENST00000442468.1:c.769G=	ENSP00000387413.1:p.Gly257=
ENST00000530231.5:c.799G=	ENSP00000433907.1:p.Gly267=
NM_000506.3:c.799G=	NP_000497.1:p.Gly267=
NM_000506.4:c.799G= , LRG_551t1:c.799G=	NP_000497.1:p.Gly267=
NM_001311257.1:c.751G=	NP_001298186.1:p.Gly251=
XR_428840.2:n.843G=
XR_428840.4:n.834G=
NM_000506.5:c.799G= MANE Select	NP_000497.1:p.Gly267=
NM_001311257.2:c.751G=	NP_001298186.1:p.Gly251=