Canonical Allele Identifier: CA1969072124

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725993C= , CM000673.2:g.46725993C=	GRCh38
NC_000011.9:g.46747543C= , CM000673.1:g.46747543C=	GRCh37
NC_000011.8:g.46704119C=	NCBI36
NG_008953.1:g.11801C= , LRG_551:g.11801C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.694C= MANE Select	ENSP00000308541.5:p.Leu232=
ENST00000311907.9:c.694C=	ENSP00000308541.5:p.Leu232=
ENST00000442468.1:c.664C=	ENSP00000387413.1:p.Leu222=
ENST00000490274.1:n.474C=
ENST00000530231.5:c.694C=	ENSP00000433907.1:p.Leu232=
NM_000506.3:c.694C=	NP_000497.1:p.Leu232=
NM_000506.4:c.694C= , LRG_551t1:c.694C=	NP_000497.1:p.Leu232=
NM_001311257.1:c.646C=	NP_001298186.1:p.Leu216=
XR_428840.2:n.738C=
XR_428840.4:n.729C=
NM_000506.5:c.694C= MANE Select	NP_000497.1:p.Leu232=
NM_001311257.2:c.646C=	NP_001298186.1:p.Leu216=