Canonical Allele Identifier: CA1969072824

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726630A= , CM000673.2:g.46726630A=	GRCh38
NC_000011.9:g.46748180A= , CM000673.1:g.46748180A=	GRCh37
NC_000011.8:g.46704756A=	NCBI36
NG_008953.1:g.12438A= , LRG_551:g.12438A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1003+4A= MANE Select	ENSP00000308541.5:n.1003+4A=
ENST00000311907.9:c.1003+4A=	ENSP00000308541.5:n.1003+4A=
ENST00000530231.5:c.1003+4A=	ENSP00000433907.1:n.1003+4A=
NM_000506.3:c.1003+4A=	NP_000497.1:n.1003+4A=
NM_000506.4:c.1003+4A= , LRG_551t1:c.1003+4A=	NP_000497.1:n.1003+4A=
NM_001311257.1:c.955+4A=	NP_001298186.1:n.955+4A=
XR_428840.2:n.1047+4A=
XR_428840.4:n.1038+4A=
NM_000506.5:c.1003+4A= MANE Select	NP_000497.1:n.1003+4A=
NM_001311257.2:c.955+4A=	NP_001298186.1:n.955+4A=