Canonical Allele Identifier: CA1969072934

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726689C= , CM000673.2:g.46726689C=	GRCh38
NC_000011.9:g.46748239C= , CM000673.1:g.46748239C=	GRCh37
NC_000011.8:g.46704815C=	NCBI36
NG_008953.1:g.12497C= , LRG_551:g.12497C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.1004-22C= MANE Select	ENSP00000308541.5:n.1004-22C=
ENST00000311907.9:c.1004-22C=	ENSP00000308541.5:n.1004-22C=
ENST00000530231.5:c.1004-22C=	ENSP00000433907.1:n.1004-22C=
NM_000506.3:c.1004-22C=	NP_000497.1:n.1004-22C=
NM_000506.4:c.1004-22C= , LRG_551t1:c.1004-22C=	NP_000497.1:n.1004-22C=
NM_001311257.1:c.956-22C=	NP_001298186.1:n.956-22C=
XR_428840.2:n.1048-22C=
XR_428840.4:n.1039-22C=
NM_000506.5:c.1004-22C= MANE Select	NP_000497.1:n.1004-22C=
NM_001311257.2:c.956-22C=	NP_001298186.1:n.956-22C=