Canonical Allele Identifier: CA474043680

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747530G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725980G>C , CM000673.2:g.46725980G>C	GRCh38
NC_000011.9:g.46747530G>C , CM000673.1:g.46747530G>C	GRCh37
NC_000011.8:g.46704106G>C	NCBI36
NG_008953.1:g.11788G>C , LRG_551:g.11788G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.681G>C MANE Select	ENSP00000308541.5:p.Val227=
ENST00000311907.9:c.681G>C	ENSP00000308541.5:p.Val227=
ENST00000442468.1:c.651G>C	ENSP00000387413.1:p.Val217=
ENST00000490274.1:n.461G>C
ENST00000530231.5:c.681G>C	ENSP00000433907.1:p.Val227=
NM_000506.3:c.681G>C	NP_000497.1:p.Val227=
NM_000506.4:c.681G>C , LRG_551t1:c.681G>C	NP_000497.1:p.Val227=
NM_001311257.1:c.633G>C	NP_001298186.1:p.Val211=
XR_428840.2:n.725G>C
XR_428840.4:n.716G>C
NM_000506.5:c.681G>C MANE Select	NP_000497.1:p.Val227=
NM_001311257.2:c.633G>C	NP_001298186.1:p.Val211=