Canonical Allele Identifier: CA421735123

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169495194C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525956C>T , CM000663.2:g.169525956C>T	GRCh38
NC_000001.10:g.169495194C>T , CM000663.1:g.169495194C>T	GRCh37
NC_000001.9:g.167761818C>T	NCBI36
NG_011806.1:g.65576G>A , LRG_553:g.65576G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5661G>A MANE Select	ENSP00000356771.3:p.Glu1887=
ENST00000367796.3:c.5676G>A	ENSP00000356770.3:p.Glu1892=
ENST00000367797.7:c.5661G>A	ENSP00000356771.3:p.Glu1887=
NM_000130.4:c.5661G>A , LRG_553t1:c.5661G>A	NP_000121.2:p.Glu1887=
XM_017000660.2:c.5250G>A	XP_016856149.1:p.Glu1750=
NM_000130.5:c.5661G>A MANE Select	NP_000121.2:p.Glu1887=