Canonical Allele Identifier: CA474043391

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747443C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725893C>G , CM000673.2:g.46725893C>G	GRCh38
NC_000011.9:g.46747443C>G , CM000673.1:g.46747443C>G	GRCh37
NC_000011.8:g.46704019C>G	NCBI36
NG_008953.1:g.11701C>G , LRG_551:g.11701C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.594C>G MANE Select	ENSP00000308541.5:p.Arg198=
ENST00000311907.9:c.594C>G	ENSP00000308541.5:p.Arg198=
ENST00000442468.1:c.564C>G	ENSP00000387413.1:p.Arg188=
ENST00000490274.1:n.374C>G
ENST00000530231.5:c.594C>G	ENSP00000433907.1:p.Arg198=
NM_000506.3:c.594C>G	NP_000497.1:p.Arg198=
NM_000506.4:c.594C>G , LRG_551t1:c.594C>G	NP_000497.1:p.Arg198=
NM_001311257.1:c.546C>G	NP_001298186.1:p.Arg182=
XR_428840.2:n.638C>G
XR_428840.4:n.629C>G
NM_000506.5:c.594C>G MANE Select	NP_000497.1:p.Arg198=
NM_001311257.2:c.546C>G	NP_001298186.1:p.Arg182=