Canonical Allele Identifier: CA380267070

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46748167G>A (hg19) ; chr11:g.46726617G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726617G>A , CM000673.2:g.46726617G>A	GRCh38
NC_000011.9:g.46748167G>A , CM000673.1:g.46748167G>A	GRCh37
NC_000011.8:g.46704743G>A	NCBI36
NG_008953.1:g.12425G>A , LRG_551:g.12425G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.994G>A MANE Select	ENSP00000308541.5:p.Gly332Arg
ENST00000311907.9:c.994G>A	ENSP00000308541.5:p.Gly332Arg
ENST00000442468.1:c.964G>A	ENSP00000387413.1:p.Gly322Arg
ENST00000530231.5:c.994G>A	ENSP00000433907.1:p.Gly332Arg
NM_000506.3:c.994G>A	NP_000497.1:p.Gly332Arg
NM_000506.4:c.994G>A , LRG_551t1:c.994G>A	NP_000497.1:p.Gly332Arg
NM_001311257.1:c.946G>A	NP_001298186.1:p.Gly316Arg
XR_428840.2:n.1038G>A
XR_428840.4:n.1029G>A
NM_000506.5:c.994G>A MANE Select	NP_000497.1:p.Gly332Arg
NM_001311257.2:c.946G>A	NP_001298186.1:p.Gly316Arg