Canonical Allele Identifier: CA473871704

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46749588T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728038T>C , CM000673.2:g.46728038T>C	GRCh38
NC_000011.9:g.46749588T>C , CM000673.1:g.46749588T>C	GRCh37
NC_000011.8:g.46706164T>C	NCBI36
NG_008953.1:g.13846T>C , LRG_551:g.13846T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1173T>C MANE Select	ENSP00000308541.5:p.Cys391=
ENST00000311907.9:c.1173T>C	ENSP00000308541.5:p.Cys391=
ENST00000530231.5:c.1173T>C	ENSP00000433907.1:p.Cys391=
NM_000506.3:c.1173T>C	NP_000497.1:p.Cys391=
NM_000506.4:c.1173T>C , LRG_551t1:c.1173T>C	NP_000497.1:p.Cys391=
NM_001311257.1:c.1125T>C	NP_001298186.1:p.Cys375=
XR_428840.2:n.1217T>C
XR_428840.4:n.1208T>C
NM_000506.5:c.1173T>C MANE Select	NP_000497.1:p.Cys391=
NM_001311257.2:c.1125T>C	NP_001298186.1:p.Cys375=