Canonical Allele Identifier: CA1969071920

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725881G= , CM000673.2:g.46725881G=	GRCh38
NC_000011.9:g.46747431G= , CM000673.1:g.46747431G=	GRCh37
NC_000011.8:g.46704007G=	NCBI36
NG_008953.1:g.11689G= , LRG_551:g.11689G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.582G= MANE Select	ENSP00000308541.5:p.Ala194=
ENST00000311907.9:c.582G=	ENSP00000308541.5:p.Ala194=
ENST00000442468.1:c.552G=	ENSP00000387413.1:p.Ala184=
ENST00000490274.1:n.362G=
ENST00000530231.5:c.582G=	ENSP00000433907.1:p.Ala194=
NM_000506.3:c.582G=	NP_000497.1:p.Ala194=
NM_000506.4:c.582G= , LRG_551t1:c.582G=	NP_000497.1:p.Ala194=
NM_001311257.1:c.534G=	NP_001298186.1:p.Ala178=
XR_428840.2:n.626G=
XR_428840.4:n.617G=
NM_000506.5:c.582G= MANE Select	NP_000497.1:p.Ala194=
NM_001311257.2:c.534G=	NP_001298186.1:p.Ala178=