Canonical Allele Identifier: CA380263172

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46745003C>A (hg19) ; chr11:g.46723453C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723453C>A , CM000673.2:g.46723453C>A	GRCh38
NC_000011.9:g.46745003C>A , CM000673.1:g.46745003C>A	GRCh37
NC_000011.8:g.46701579C>A	NCBI36
NG_008953.1:g.9261C>A , LRG_551:g.9261C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.494C>A MANE Select	ENSP00000308541.5:p.Thr165Lys
ENST00000311907.9:c.494C>A	ENSP00000308541.5:p.Thr165Lys
ENST00000442468.1:c.464C>A	ENSP00000387413.1:p.Thr155Lys
ENST00000490274.1:n.274C>A
ENST00000530231.5:c.494C>A	ENSP00000433907.1:p.Thr165Lys
NM_000506.3:c.494C>A	NP_000497.1:p.Thr165Lys
NM_000506.4:c.494C>A , LRG_551t1:c.494C>A	NP_000497.1:p.Thr165Lys
NM_001311257.1:c.446C>A	NP_001298186.1:p.Thr149Lys
XR_428840.2:n.538C>A
XR_428840.4:n.529C>A
NM_000506.5:c.494C>A MANE Select	NP_000497.1:p.Thr165Lys
NM_001311257.2:c.446C>A	NP_001298186.1:p.Thr149Lys