Canonical Allele Identifier: CA380264705

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747435A>T (hg19) ; chr11:g.46725885A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725885A>T , CM000673.2:g.46725885A>T	GRCh38
NC_000011.9:g.46747435A>T , CM000673.1:g.46747435A>T	GRCh37
NC_000011.8:g.46704011A>T	NCBI36
NG_008953.1:g.11693A>T , LRG_551:g.11693A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.586A>T MANE Select	ENSP00000308541.5:p.Thr196Ser
ENST00000311907.9:c.586A>T	ENSP00000308541.5:p.Thr196Ser
ENST00000442468.1:c.556A>T	ENSP00000387413.1:p.Thr186Ser
ENST00000490274.1:n.366A>T
ENST00000530231.5:c.586A>T	ENSP00000433907.1:p.Thr196Ser
NM_000506.3:c.586A>T	NP_000497.1:p.Thr196Ser
NM_000506.4:c.586A>T , LRG_551t1:c.586A>T	NP_000497.1:p.Thr196Ser
NM_001311257.1:c.538A>T	NP_001298186.1:p.Thr180Ser
XR_428840.2:n.630A>T
XR_428840.4:n.621A>T
NM_000506.5:c.586A>T MANE Select	NP_000497.1:p.Thr196Ser
NM_001311257.2:c.538A>T	NP_001298186.1:p.Thr180Ser