Canonical Allele Identifier: CA474043478

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46748067G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726517G>A , CM000673.2:g.46726517G>A	GRCh38
NC_000011.9:g.46748067G>A , CM000673.1:g.46748067G>A	GRCh37
NC_000011.8:g.46704643G>A	NCBI36
NG_008953.1:g.12325G>A , LRG_551:g.12325G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.894G>A MANE Select	ENSP00000308541.5:p.Glu298=
ENST00000311907.9:c.894G>A	ENSP00000308541.5:p.Glu298=
ENST00000442468.1:c.864G>A	ENSP00000387413.1:p.Glu288=
ENST00000530231.5:c.894G>A	ENSP00000433907.1:p.Glu298=
NM_000506.3:c.894G>A	NP_000497.1:p.Glu298=
NM_000506.4:c.894G>A , LRG_551t1:c.894G>A	NP_000497.1:p.Glu298=
NM_001311257.1:c.846G>A	NP_001298186.1:p.Glu282=
XR_428840.2:n.938G>A
XR_428840.4:n.929G>A
NM_000506.5:c.894G>A MANE Select	NP_000497.1:p.Glu298=
NM_001311257.2:c.846G>A	NP_001298186.1:p.Glu282=