Canonical Allele Identifier: CA1969074101

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728143T= , CM000673.2:g.46728143T=	GRCh38
NC_000011.9:g.46749693T= , CM000673.1:g.46749693T=	GRCh37
NC_000011.8:g.46706269T=	NCBI36
NG_008953.1:g.13951T= , LRG_551:g.13951T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1278T= MANE Select	ENSP00000308541.5:p.Ile426=
ENST00000311907.9:c.1278T=	ENSP00000308541.5:p.Ile426=
ENST00000530231.5:c.1278T=	ENSP00000433907.1:p.Ile426=
NM_000506.3:c.1278T=	NP_000497.1:p.Ile426=
NM_000506.4:c.1278T= , LRG_551t1:c.1278T=	NP_000497.1:p.Ile426=
NM_001311257.1:c.1230T=	NP_001298186.1:p.Ile410=
XR_428840.2:n.1322T=
XR_428840.4:n.1313T=
NM_000506.5:c.1278T= MANE Select	NP_000497.1:p.Ile426=
NM_001311257.2:c.1230T=	NP_001298186.1:p.Ile410=