Canonical Allele Identifier: CA380259622

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46739326G>A , CM000673.2:g.46739326G>A	GRCh38
NC_000011.9:g.46760876G>A , CM000673.1:g.46760876G>A	GRCh37
NC_000011.8:g.46717452G>A	NCBI36
NG_008953.1:g.25134G>A , LRG_551:g.25134G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000506.5:c.1787G>A MANE Select	NP_000497.1:p.Arg596Gln
ENST00000311907.10:c.1787G>A MANE Select	ENSP00000308541.5:p.Arg596Gln
NM_000506.3:c.1787G>A	NP_000497.1:p.Arg596Gln
NM_000506.4:c.1787G>A , LRG_551t1:c.1787G>A	NP_000497.1:p.Arg596Gln
NM_001311257.1:c.1739G>A	NP_001298186.1:p.Arg580Gln
NM_001311257.2:c.1739G>A	NP_001298186.1:p.Arg580Gln
ENST00000311907.9:c.1787G>A	ENSP00000308541.5:p.Arg596Gln
ENST00000530231.5:c.1670G>A	ENSP00000433907.1:p.Arg557Gln
XR_428840.2:n.1649G>A
XR_428840.4:n.1640G>A