Canonical Allele Identifier: CA474043692

Gene: F2

Linked Data

• COSMIC: COSM5530722
• MyVariant Identifiers: chr11:g.46747533C>T (hg19)

Genomic Alleles

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

Transcript Alleles

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