Canonical Allele Identifier: CA1969074197

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728192G= , CM000673.2:g.46728192G=	GRCh38
NC_000011.9:g.46749742G= , CM000673.1:g.46749742G=	GRCh37
NC_000011.8:g.46706318G=	NCBI36
NG_008953.1:g.14000G= , LRG_551:g.14000G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1298+29G= MANE Select	ENSP00000308541.5:n.1298+29G=
ENST00000311907.9:c.1298+29G=	ENSP00000308541.5:n.1298+29G=
ENST00000530231.5:c.1298+29G=	ENSP00000433907.1:n.1298+29G=
NM_000506.3:c.1298+29G=	NP_000497.1:n.1298+29G=
NM_000506.4:c.1298+29G= , LRG_551t1:c.1298+29G=	NP_000497.1:n.1298+29G=
NM_001311257.1:c.1250+29G=	NP_001298186.1:n.1250+29G=
XR_428840.2:n.1342+29G=
XR_428840.4:n.1333+29G=
NM_000506.5:c.1298+29G= MANE Select	NP_000497.1:n.1298+29G=
NM_001311257.2:c.1250+29G=	NP_001298186.1:n.1250+29G=