Canonical Allele Identifier: CA474043559

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46748091C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726541C>T , CM000673.2:g.46726541C>T	GRCh38
NC_000011.9:g.46748091C>T , CM000673.1:g.46748091C>T	GRCh37
NC_000011.8:g.46704667C>T	NCBI36
NG_008953.1:g.12349C>T , LRG_551:g.12349C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.918C>T MANE Select	ENSP00000308541.5:p.Asp306=
ENST00000311907.9:c.918C>T	ENSP00000308541.5:p.Asp306=
ENST00000442468.1:c.888C>T	ENSP00000387413.1:p.Asp296=
ENST00000530231.5:c.918C>T	ENSP00000433907.1:p.Asp306=
NM_000506.3:c.918C>T	NP_000497.1:p.Asp306=
NM_000506.4:c.918C>T , LRG_551t1:c.918C>T	NP_000497.1:p.Asp306=
NM_001311257.1:c.870C>T	NP_001298186.1:p.Asp290=
XR_428840.2:n.962C>T
XR_428840.4:n.953C>T
NM_000506.5:c.918C>T MANE Select	NP_000497.1:p.Asp306=
NM_001311257.2:c.870C>T	NP_001298186.1:p.Asp290=