Canonical Allele Identifier: CA1969072386

Gene: F2

Linked Data

• ClinVar Variation Id: 2860424
• ClinVar RCV Id: RCV003626207
• dbSNP Id: rs2064871675

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726193_46726208dup , CM000673.2:g.46726193_46726208dup	GRCh38
NC_000011.9:g.46747743_46747758dup , CM000673.1:g.46747743_46747758dup	GRCh37
NC_000011.8:g.46704319_46704334dup	NCBI36
NG_008953.1:g.12001_12016dup , LRG_551:g.12001_12016dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+20_874+35dup MANE Select	ENSP00000308541.5:n.874+20_874+35dup
ENST00000311907.9:c.874+20_874+35dup	ENSP00000308541.5:n.874+20_874+35dup
ENST00000442468.1:c.844+20_844+35dup	ENSP00000387413.1:n.844+20_844+35dup
ENST00000530231.5:c.874+20_874+35dup	ENSP00000433907.1:n.874+20_874+35dup
NM_000506.3:c.874+20_874+35dup	NP_000497.1:n.874+20_874+35dup
NM_000506.4:c.874+20_874+35dup , LRG_551t1:c.874+20_874+35dup	NP_000497.1:n.874+20_874+35dup
NM_001311257.1:c.826+20_826+35dup	NP_001298186.1:n.826+20_826+35dup
XR_428840.2:n.918+20_918+35dup
XR_428840.4:n.909+20_909+35dup
NM_000506.5:c.874+20_874+35dup MANE Select	NP_000497.1:n.874+20_874+35dup
NM_001311257.2:c.826+20_826+35dup	NP_001298186.1:n.826+20_826+35dup