Canonical Allele Identifier: CA380262947

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723408C>T , CM000673.2:g.46723408C>T	GRCh38
NC_000011.9:g.46744958C>T , CM000673.1:g.46744958C>T	GRCh37
NC_000011.8:g.46701534C>T	NCBI36
NG_008953.1:g.9216C>T , LRG_551:g.9216C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.449C>T MANE Select	ENSP00000308541.5:p.Ala150Val
ENST00000311907.9:c.449C>T	ENSP00000308541.5:p.Ala150Val
ENST00000442468.1:c.419C>T	ENSP00000387413.1:p.Ala140Val
ENST00000490274.1:n.229C>T
ENST00000530231.5:c.449C>T	ENSP00000433907.1:p.Ala150Val
NM_000506.3:c.449C>T	NP_000497.1:p.Ala150Val
NM_000506.4:c.449C>T , LRG_551t1:c.449C>T	NP_000497.1:p.Ala150Val
NM_001311257.1:c.401C>T	NP_001298186.1:p.Ala134Val
XR_428840.2:n.493C>T
XR_428840.4:n.484C>T
NM_000506.5:c.449C>T MANE Select	NP_000497.1:p.Ala150Val
NM_001311257.2:c.401C>T	NP_001298186.1:p.Ala134Val