Canonical Allele Identifier: CA474043720

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747551C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726001C>T , CM000673.2:g.46726001C>T	GRCh38
NC_000011.9:g.46747551C>T , CM000673.1:g.46747551C>T	GRCh37
NC_000011.8:g.46704127C>T	NCBI36
NG_008953.1:g.11809C>T , LRG_551:g.11809C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.702C>T MANE Select	ENSP00000308541.5:p.Cys234=
ENST00000311907.9:c.702C>T	ENSP00000308541.5:p.Cys234=
ENST00000442468.1:c.672C>T	ENSP00000387413.1:p.Cys224=
ENST00000490274.1:n.482C>T
ENST00000530231.5:c.702C>T	ENSP00000433907.1:p.Cys234=
NM_000506.3:c.702C>T	NP_000497.1:p.Cys234=
NM_000506.4:c.702C>T , LRG_551t1:c.702C>T	NP_000497.1:p.Cys234=
NM_001311257.1:c.654C>T	NP_001298186.1:p.Cys218=
XR_428840.2:n.746C>T
XR_428840.4:n.737C>T
NM_000506.5:c.702C>T MANE Select	NP_000497.1:p.Cys234=
NM_001311257.2:c.654C>T	NP_001298186.1:p.Cys218=