Canonical Allele Identifier: CA474043695

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46748169A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726619A>T , CM000673.2:g.46726619A>T	GRCh38
NC_000011.9:g.46748169A>T , CM000673.1:g.46748169A>T	GRCh37
NC_000011.8:g.46704745A>T	NCBI36
NG_008953.1:g.12427A>T , LRG_551:g.12427A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.996A>T MANE Select	ENSP00000308541.5:p.Gly332=
ENST00000311907.9:c.996A>T	ENSP00000308541.5:p.Gly332=
ENST00000442468.1:c.966A>T	ENSP00000387413.1:p.Gly322=
ENST00000530231.5:c.996A>T	ENSP00000433907.1:p.Gly332=
NM_000506.3:c.996A>T	NP_000497.1:p.Gly332=
NM_000506.4:c.996A>T , LRG_551t1:c.996A>T	NP_000497.1:p.Gly332=
NM_001311257.1:c.948A>T	NP_001298186.1:p.Gly316=
XR_428840.2:n.1040A>T
XR_428840.4:n.1031A>T
NM_000506.5:c.996A>T MANE Select	NP_000497.1:p.Gly332=
NM_001311257.2:c.948A>T	NP_001298186.1:p.Gly316=