Canonical Allele Identifier: CA380262890

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723398C>G , CM000673.2:g.46723398C>G	GRCh38
NC_000011.9:g.46744948C>G , CM000673.1:g.46744948C>G	GRCh37
NC_000011.8:g.46701524C>G	NCBI36
NG_008953.1:g.9206C>G , LRG_551:g.9206C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.439C>G MANE Select	ENSP00000308541.5:p.His147Asp
ENST00000311907.9:c.439C>G	ENSP00000308541.5:p.His147Asp
ENST00000442468.1:c.409C>G	ENSP00000387413.1:p.His137Asp
ENST00000490274.1:n.219C>G
ENST00000530231.5:c.439C>G	ENSP00000433907.1:p.His147Asp
NM_000506.3:c.439C>G	NP_000497.1:p.His147Asp
NM_000506.4:c.439C>G , LRG_551t1:c.439C>G	NP_000497.1:p.His147Asp
NM_001311257.1:c.391C>G	NP_001298186.1:p.His131Asp
XR_428840.2:n.483C>G
XR_428840.4:n.474C>G
NM_000506.5:c.439C>G MANE Select	NP_000497.1:p.His147Asp
NM_001311257.2:c.391C>G	NP_001298186.1:p.His131Asp