Canonical Allele Identifier: CA2791314709

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723376T>G , CM000673.2:g.46723376T>G	GRCh38
NC_000011.9:g.46744926T>G , CM000673.1:g.46744926T>G	GRCh37
NC_000011.8:g.46701502T>G	NCBI36
NG_008953.1:g.9184T>G , LRG_551:g.9184T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.423-6T>G MANE Select	ENSP00000308541.5:n.423-6T>G
ENST00000311907.9:c.423-6T>G	ENSP00000308541.5:n.423-6T>G
ENST00000442468.1:c.393-6T>G	ENSP00000387413.1:n.393-6T>G
ENST00000490274.1:n.197T>G
ENST00000530231.5:c.423-6T>G	ENSP00000433907.1:n.423-6T>G
NM_000506.3:c.423-6T>G	NP_000497.1:n.423-6T>G
NM_000506.4:c.423-6T>G , LRG_551t1:c.423-6T>G	NP_000497.1:n.423-6T>G
NM_001311257.1:c.375-6T>G	NP_001298186.1:n.375-6T>G
XR_428840.2:n.467-6T>G
XR_428840.4:n.458-6T>G
NM_000506.5:c.423-6T>G MANE Select	NP_000497.1:n.423-6T>G
NM_001311257.2:c.375-6T>G	NP_001298186.1:n.375-6T>G