Canonical Allele Identifier: CA380264939

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747507C>T (hg19) ; chr11:g.46725957C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725957C>T , CM000673.2:g.46725957C>T	GRCh38
NC_000011.9:g.46747507C>T , CM000673.1:g.46747507C>T	GRCh37
NC_000011.8:g.46704083C>T	NCBI36
NG_008953.1:g.11765C>T , LRG_551:g.11765C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.658C>T MANE Select	ENSP00000308541.5:p.Gln220Ter
ENST00000311907.9:c.658C>T	ENSP00000308541.5:p.Gln220Ter
ENST00000442468.1:c.628C>T	ENSP00000387413.1:p.Gln210Ter
ENST00000490274.1:n.438C>T
ENST00000530231.5:c.658C>T	ENSP00000433907.1:p.Gln220Ter
NM_000506.3:c.658C>T	NP_000497.1:p.Gln220Ter
NM_000506.4:c.658C>T , LRG_551t1:c.658C>T	NP_000497.1:p.Gln220Ter
NM_001311257.1:c.610C>T	NP_001298186.1:p.Gln204Ter
XR_428840.2:n.702C>T
XR_428840.4:n.693C>T
NM_000506.5:c.658C>T MANE Select	NP_000497.1:p.Gln220Ter
NM_001311257.2:c.610C>T	NP_001298186.1:p.Gln204Ter