Canonical Allele Identifier: CA1969074039

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728089C= , CM000673.2:g.46728089C=	GRCh38
NC_000011.9:g.46749639C= , CM000673.1:g.46749639C=	GRCh37
NC_000011.8:g.46706215C=	NCBI36
NG_008953.1:g.13897C= , LRG_551:g.13897C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1224C= MANE Select	ENSP00000308541.5:p.Leu408=
ENST00000311907.9:c.1224C=	ENSP00000308541.5:p.Leu408=
ENST00000530231.5:c.1224C=	ENSP00000433907.1:p.Leu408=
NM_000506.3:c.1224C=	NP_000497.1:p.Leu408=
NM_000506.4:c.1224C= , LRG_551t1:c.1224C=	NP_000497.1:p.Leu408=
NM_001311257.1:c.1176C=	NP_001298186.1:p.Leu392=
XR_428840.2:n.1268C=
XR_428840.4:n.1259C=
NM_000506.5:c.1224C= MANE Select	NP_000497.1:p.Leu408=
NM_001311257.2:c.1176C=	NP_001298186.1:p.Leu392=