Canonical Allele Identifier: CA474043432

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747452C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725902C>A , CM000673.2:g.46725902C>A	GRCh38
NC_000011.9:g.46747452C>A , CM000673.1:g.46747452C>A	GRCh37
NC_000011.8:g.46704028C>A	NCBI36
NG_008953.1:g.11710C>A , LRG_551:g.11710C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.603C>A MANE Select	ENSP00000308541.5:p.Gly201=
ENST00000311907.9:c.603C>A	ENSP00000308541.5:p.Gly201=
ENST00000442468.1:c.573C>A	ENSP00000387413.1:p.Gly191=
ENST00000490274.1:n.383C>A
ENST00000530231.5:c.603C>A	ENSP00000433907.1:p.Gly201=
NM_000506.3:c.603C>A	NP_000497.1:p.Gly201=
NM_000506.4:c.603C>A , LRG_551t1:c.603C>A	NP_000497.1:p.Gly201=
NM_001311257.1:c.555C>A	NP_001298186.1:p.Gly185=
XR_428840.2:n.647C>A
XR_428840.4:n.638C>A
NM_000506.5:c.603C>A MANE Select	NP_000497.1:p.Gly201=
NM_001311257.2:c.555C>A	NP_001298186.1:p.Gly185=