Canonical Allele Identifier: CA1969074078

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728126G= , CM000673.2:g.46728126G=	GRCh38
NC_000011.9:g.46749676G= , CM000673.1:g.46749676G=	GRCh37
NC_000011.8:g.46706252G=	NCBI36
NG_008953.1:g.13934G= , LRG_551:g.13934G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1261G= MANE Select	ENSP00000308541.5:p.Asp421=
ENST00000311907.9:c.1261G=	ENSP00000308541.5:p.Asp421=
ENST00000530231.5:c.1261G=	ENSP00000433907.1:p.Asp421=
NM_000506.3:c.1261G=	NP_000497.1:p.Asp421=
NM_000506.4:c.1261G= , LRG_551t1:c.1261G=	NP_000497.1:p.Asp421=
NM_001311257.1:c.1213G=	NP_001298186.1:p.Asp405=
XR_428840.2:n.1305G=
XR_428840.4:n.1296G=
NM_000506.5:c.1261G= MANE Select	NP_000497.1:p.Asp421=
NM_001311257.2:c.1213G=	NP_001298186.1:p.Asp405=