Canonical Allele Identifier: CA380265099

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747552C>A (hg19) ; chr11:g.46726002C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726002C>A , CM000673.2:g.46726002C>A	GRCh38
NC_000011.9:g.46747552C>A , CM000673.1:g.46747552C>A	GRCh37
NC_000011.8:g.46704128C>A	NCBI36
NG_008953.1:g.11810C>A , LRG_551:g.11810C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.703C>A MANE Select	ENSP00000308541.5:p.Leu235Met
ENST00000311907.9:c.703C>A	ENSP00000308541.5:p.Leu235Met
ENST00000442468.1:c.673C>A	ENSP00000387413.1:p.Leu225Met
ENST00000490274.1:n.483C>A
ENST00000530231.5:c.703C>A	ENSP00000433907.1:p.Leu235Met
NM_000506.3:c.703C>A	NP_000497.1:p.Leu235Met
NM_000506.4:c.703C>A , LRG_551t1:c.703C>A	NP_000497.1:p.Leu235Met
NM_001311257.1:c.655C>A	NP_001298186.1:p.Leu219Met
XR_428840.2:n.747C>A
XR_428840.4:n.738C>A
NM_000506.5:c.703C>A MANE Select	NP_000497.1:p.Leu235Met
NM_001311257.2:c.655C>A	NP_001298186.1:p.Leu219Met