Canonical Allele Identifier: CA474043502

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46748070A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726520A>G , CM000673.2:g.46726520A>G	GRCh38
NC_000011.9:g.46748070A>G , CM000673.1:g.46748070A>G	GRCh37
NC_000011.8:g.46704646A>G	NCBI36
NG_008953.1:g.12328A>G , LRG_551:g.12328A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.897A>G MANE Select	ENSP00000308541.5:p.Thr299=
ENST00000311907.9:c.897A>G	ENSP00000308541.5:p.Thr299=
ENST00000442468.1:c.867A>G	ENSP00000387413.1:p.Thr289=
ENST00000530231.5:c.897A>G	ENSP00000433907.1:p.Thr299=
NM_000506.3:c.897A>G	NP_000497.1:p.Thr299=
NM_000506.4:c.897A>G , LRG_551t1:c.897A>G	NP_000497.1:p.Thr299=
NM_001311257.1:c.849A>G	NP_001298186.1:p.Thr283=
XR_428840.2:n.941A>G
XR_428840.4:n.932A>G
NM_000506.5:c.897A>G MANE Select	NP_000497.1:p.Thr299=
NM_001311257.2:c.849A>G	NP_001298186.1:p.Thr283=