Canonical Allele Identifier: CA343124922

Gene: F5

Linked Data

• dbSNP Id: rs1659436283
• MyVariant Identifiers: chr1:g.169495195T>C (hg19) ; chr1:g.169525957T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525957T>C , CM000663.2:g.169525957T>C	GRCh38
NC_000001.10:g.169495195T>C , CM000663.1:g.169495195T>C	GRCh37
NC_000001.9:g.167761819T>C	NCBI36
NG_011806.1:g.65575A>G , LRG_553:g.65575A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5660A>G MANE Select	ENSP00000356771.3:p.Glu1887Gly
ENST00000367796.3:c.5675A>G	ENSP00000356770.3:p.Glu1892Gly
ENST00000367797.7:c.5660A>G	ENSP00000356771.3:p.Glu1887Gly
NM_000130.4:c.5660A>G , LRG_553t1:c.5660A>G	NP_000121.2:p.Glu1887Gly
XM_017000660.2:c.5249A>G	XP_016856149.1:p.Glu1750Gly
NM_000130.5:c.5660A>G MANE Select	NP_000121.2:p.Glu1887Gly