Canonical Allele Identifier: CA380264948

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747510T>A (hg19) ; chr11:g.46725960T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725960T>A , CM000673.2:g.46725960T>A	GRCh38
NC_000011.9:g.46747510T>A , CM000673.1:g.46747510T>A	GRCh37
NC_000011.8:g.46704086T>A	NCBI36
NG_008953.1:g.11768T>A , LRG_551:g.11768T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.661T>A MANE Select	ENSP00000308541.5:p.Tyr221Asn
ENST00000311907.9:c.661T>A	ENSP00000308541.5:p.Tyr221Asn
ENST00000442468.1:c.631T>A	ENSP00000387413.1:p.Tyr211Asn
ENST00000490274.1:n.441T>A
ENST00000530231.5:c.661T>A	ENSP00000433907.1:p.Tyr221Asn
NM_000506.3:c.661T>A	NP_000497.1:p.Tyr221Asn
NM_000506.4:c.661T>A , LRG_551t1:c.661T>A	NP_000497.1:p.Tyr221Asn
NM_001311257.1:c.613T>A	NP_001298186.1:p.Tyr205Asn
XR_428840.2:n.705T>A
XR_428840.4:n.696T>A
NM_000506.5:c.661T>A MANE Select	NP_000497.1:p.Tyr221Asn
NM_001311257.2:c.613T>A	NP_001298186.1:p.Tyr205Asn