Canonical Allele Identifier: CA1969072030

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725945G= , CM000673.2:g.46725945G=	GRCh38
NC_000011.9:g.46747495G= , CM000673.1:g.46747495G=	GRCh37
NC_000011.8:g.46704071G=	NCBI36
NG_008953.1:g.11753G= , LRG_551:g.11753G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.646G= MANE Select	ENSP00000308541.5:p.Asp216=
ENST00000311907.9:c.646G=	ENSP00000308541.5:p.Asp216=
ENST00000442468.1:c.616G=	ENSP00000387413.1:p.Asp206=
ENST00000490274.1:n.426G=
ENST00000530231.5:c.646G=	ENSP00000433907.1:p.Asp216=
NM_000506.3:c.646G=	NP_000497.1:p.Asp216=
NM_000506.4:c.646G= , LRG_551t1:c.646G=	NP_000497.1:p.Asp216=
NM_001311257.1:c.598G=	NP_001298186.1:p.Asp200=
XR_428840.2:n.690G=
XR_428840.4:n.681G=
NM_000506.5:c.646G= MANE Select	NP_000497.1:p.Asp216=
NM_001311257.2:c.598G=	NP_001298186.1:p.Asp200=