Canonical Allele Identifier: CA380267677

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726761G>T , CM000673.2:g.46726761G>T	GRCh38
NC_000011.9:g.46748311G>T , CM000673.1:g.46748311G>T	GRCh37
NC_000011.8:g.46704887G>T	NCBI36
NG_008953.1:g.12569G>T , LRG_551:g.12569G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000506.5:c.1054G>T MANE Select	NP_000497.1:p.Glu352Ter
ENST00000311907.10:c.1054G>T MANE Select	ENSP00000308541.5:p.Glu352Ter
NM_000506.3:c.1054G>T	NP_000497.1:p.Glu352Ter
NM_000506.4:c.1054G>T , LRG_551t1:c.1054G>T	NP_000497.1:p.Glu352Ter
NM_001311257.1:c.1006G>T	NP_001298186.1:p.Glu336Ter
NM_001311257.2:c.1006G>T	NP_001298186.1:p.Glu336Ter
ENST00000311907.9:c.1054G>T	ENSP00000308541.5:p.Glu352Ter
ENST00000530231.5:c.1054G>T	ENSP00000433907.1:p.Glu352Ter
XR_428840.2:n.1098G>T
XR_428840.4:n.1089G>T