Canonical Allele Identifier: CA474043732

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747563C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726013C>A , CM000673.2:g.46726013C>A	GRCh38
NC_000011.9:g.46747563C>A , CM000673.1:g.46747563C>A	GRCh37
NC_000011.8:g.46704139C>A	NCBI36
NG_008953.1:g.11821C>A , LRG_551:g.11821C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.714C>A MANE Select	ENSP00000308541.5:p.Ala238=
ENST00000311907.9:c.714C>A	ENSP00000308541.5:p.Ala238=
ENST00000442468.1:c.684C>A	ENSP00000387413.1:p.Ala228=
ENST00000490274.1:n.494C>A
ENST00000530231.5:c.714C>A	ENSP00000433907.1:p.Ala238=
NM_000506.3:c.714C>A	NP_000497.1:p.Ala238=
NM_000506.4:c.714C>A , LRG_551t1:c.714C>A	NP_000497.1:p.Ala238=
NM_001311257.1:c.666C>A	NP_001298186.1:p.Ala222=
XR_428840.2:n.758C>A
XR_428840.4:n.749C>A
NM_000506.5:c.714C>A MANE Select	NP_000497.1:p.Ala238=
NM_001311257.2:c.666C>A	NP_001298186.1:p.Ala222=