Canonical Allele Identifier: CA474043689

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747533C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725983C>A , CM000673.2:g.46725983C>A	GRCh38
NC_000011.9:g.46747533C>A , CM000673.1:g.46747533C>A	GRCh37
NC_000011.8:g.46704109C>A	NCBI36
NG_008953.1:g.11791C>A , LRG_551:g.11791C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.684C>A MANE Select	ENSP00000308541.5:p.Thr228=
ENST00000311907.9:c.684C>A	ENSP00000308541.5:p.Thr228=
ENST00000442468.1:c.654C>A	ENSP00000387413.1:p.Thr218=
ENST00000490274.1:n.464C>A
ENST00000530231.5:c.684C>A	ENSP00000433907.1:p.Thr228=
NM_000506.3:c.684C>A	NP_000497.1:p.Thr228=
NM_000506.4:c.684C>A , LRG_551t1:c.684C>A	NP_000497.1:p.Thr228=
NM_001311257.1:c.636C>A	NP_001298186.1:p.Thr212=
XR_428840.2:n.728C>A
XR_428840.4:n.719C>A
NM_000506.5:c.684C>A MANE Select	NP_000497.1:p.Thr228=
NM_001311257.2:c.636C>A	NP_001298186.1:p.Thr212=