Canonical Allele Identifier: CA473871938

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46749681T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728131T>A , CM000673.2:g.46728131T>A	GRCh38
NC_000011.9:g.46749681T>A , CM000673.1:g.46749681T>A	GRCh37
NC_000011.8:g.46706257T>A	NCBI36
NG_008953.1:g.13939T>A , LRG_551:g.13939T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1266T>A MANE Select	ENSP00000308541.5:p.Leu422=
ENST00000311907.9:c.1266T>A	ENSP00000308541.5:p.Leu422=
ENST00000530231.5:c.1266T>A	ENSP00000433907.1:p.Leu422=
NM_000506.3:c.1266T>A	NP_000497.1:p.Leu422=
NM_000506.4:c.1266T>A , LRG_551t1:c.1266T>A	NP_000497.1:p.Leu422=
NM_001311257.1:c.1218T>A	NP_001298186.1:p.Leu406=
XR_428840.2:n.1310T>A
XR_428840.4:n.1301T>A
NM_000506.5:c.1266T>A MANE Select	NP_000497.1:p.Leu422=
NM_001311257.2:c.1218T>A	NP_001298186.1:p.Leu406=