Canonical Allele Identifier: CA380264718

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747444T>A (hg19) ; chr11:g.46725894T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725894T>A , CM000673.2:g.46725894T>A	GRCh38
NC_000011.9:g.46747444T>A , CM000673.1:g.46747444T>A	GRCh37
NC_000011.8:g.46704020T>A	NCBI36
NG_008953.1:g.11702T>A , LRG_551:g.11702T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.595T>A MANE Select	ENSP00000308541.5:p.Ser199Thr
ENST00000311907.9:c.595T>A	ENSP00000308541.5:p.Ser199Thr
ENST00000442468.1:c.565T>A	ENSP00000387413.1:p.Ser189Thr
ENST00000490274.1:n.375T>A
ENST00000530231.5:c.595T>A	ENSP00000433907.1:p.Ser199Thr
NM_000506.3:c.595T>A	NP_000497.1:p.Ser199Thr
NM_000506.4:c.595T>A , LRG_551t1:c.595T>A	NP_000497.1:p.Ser199Thr
NM_001311257.1:c.547T>A	NP_001298186.1:p.Ser183Thr
XR_428840.2:n.639T>A
XR_428840.4:n.630T>A
NM_000506.5:c.595T>A MANE Select	NP_000497.1:p.Ser199Thr
NM_001311257.2:c.547T>A	NP_001298186.1:p.Ser183Thr