Canonical Allele Identifier: CA2739270429

Gene: F2

Linked Data

• ClinVar Variation Id: 2860823
• ClinVar RCV Id: RCV003626215

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723369T>A , CM000673.2:g.46723369T>A	GRCh38
NC_000011.9:g.46744919T>A , CM000673.1:g.46744919T>A	GRCh37
NC_000011.8:g.46701495T>A	NCBI36
NG_008953.1:g.9177T>A , LRG_551:g.9177T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.423-13T>A MANE Select	ENSP00000308541.5:n.423-13T>A
ENST00000311907.9:c.423-13T>A	ENSP00000308541.5:n.423-13T>A
ENST00000442468.1:c.393-13T>A	ENSP00000387413.1:n.393-13T>A
ENST00000490274.1:n.190T>A
ENST00000530231.5:c.423-13T>A	ENSP00000433907.1:n.423-13T>A
NM_000506.3:c.423-13T>A	NP_000497.1:n.423-13T>A
NM_000506.4:c.423-13T>A , LRG_551t1:c.423-13T>A	NP_000497.1:n.423-13T>A
NM_001311257.1:c.375-13T>A	NP_001298186.1:n.375-13T>A
XR_428840.2:n.467-13T>A
XR_428840.4:n.458-13T>A
NM_000506.5:c.423-13T>A MANE Select	NP_000497.1:n.423-13T>A
NM_001311257.2:c.375-13T>A	NP_001298186.1:n.375-13T>A