Canonical Allele Identifier: CA1969071918

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725880C= , CM000673.2:g.46725880C=	GRCh38
NC_000011.9:g.46747430C= , CM000673.1:g.46747430C=	GRCh37
NC_000011.8:g.46704006C=	NCBI36
NG_008953.1:g.11688C= , LRG_551:g.11688C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.581C= MANE Select	ENSP00000308541.5:p.Ala194=
ENST00000311907.9:c.581C=	ENSP00000308541.5:p.Ala194=
ENST00000442468.1:c.551C=	ENSP00000387413.1:p.Ala184=
ENST00000490274.1:n.361C=
ENST00000530231.5:c.581C=	ENSP00000433907.1:p.Ala194=
NM_000506.3:c.581C=	NP_000497.1:p.Ala194=
NM_000506.4:c.581C= , LRG_551t1:c.581C=	NP_000497.1:p.Ala194=
NM_001311257.1:c.533C=	NP_001298186.1:p.Ala178=
XR_428840.2:n.625C=
XR_428840.4:n.616C=
NM_000506.5:c.581C= MANE Select	NP_000497.1:p.Ala194=
NM_001311257.2:c.533C=	NP_001298186.1:p.Ala178=