Canonical Allele Identifier: CA474043543

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747476A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725926A>T , CM000673.2:g.46725926A>T	GRCh38
NC_000011.9:g.46747476A>T , CM000673.1:g.46747476A>T	GRCh37
NC_000011.8:g.46704052A>T	NCBI36
NG_008953.1:g.11734A>T , LRG_551:g.11734A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.627A>T MANE Select	ENSP00000308541.5:p.Pro209=
ENST00000311907.9:c.627A>T	ENSP00000308541.5:p.Pro209=
ENST00000442468.1:c.597A>T	ENSP00000387413.1:p.Pro199=
ENST00000490274.1:n.407A>T
ENST00000530231.5:c.627A>T	ENSP00000433907.1:p.Pro209=
NM_000506.3:c.627A>T	NP_000497.1:p.Pro209=
NM_000506.4:c.627A>T , LRG_551t1:c.627A>T	NP_000497.1:p.Pro209=
NM_001311257.1:c.579A>T	NP_001298186.1:p.Pro193=
XR_428840.2:n.671A>T
XR_428840.4:n.662A>T
NM_000506.5:c.627A>T MANE Select	NP_000497.1:p.Pro209=
NM_001311257.2:c.579A>T	NP_001298186.1:p.Pro193=