Canonical Allele Identifier: CA380264832

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747478T>A (hg19) ; chr11:g.46725928T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725928T>A , CM000673.2:g.46725928T>A	GRCh38
NC_000011.9:g.46747478T>A , CM000673.1:g.46747478T>A	GRCh37
NC_000011.8:g.46704054T>A	NCBI36
NG_008953.1:g.11736T>A , LRG_551:g.11736T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.629T>A MANE Select	ENSP00000308541.5:p.Leu210Ter
ENST00000311907.9:c.629T>A	ENSP00000308541.5:p.Leu210Ter
ENST00000442468.1:c.599T>A	ENSP00000387413.1:p.Leu200Ter
ENST00000490274.1:n.409T>A
ENST00000530231.5:c.629T>A	ENSP00000433907.1:p.Leu210Ter
NM_000506.3:c.629T>A	NP_000497.1:p.Leu210Ter
NM_000506.4:c.629T>A , LRG_551t1:c.629T>A	NP_000497.1:p.Leu210Ter
NM_001311257.1:c.581T>A	NP_001298186.1:p.Leu194Ter
XR_428840.2:n.673T>A
XR_428840.4:n.664T>A
NM_000506.5:c.629T>A MANE Select	NP_000497.1:p.Leu210Ter
NM_001311257.2:c.581T>A	NP_001298186.1:p.Leu194Ter