Canonical Allele Identifier: CA421735120

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169495191A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525953A>T , CM000663.2:g.169525953A>T	GRCh38
NC_000001.10:g.169495191A>T , CM000663.1:g.169495191A>T	GRCh37
NC_000001.9:g.167761815A>T	NCBI36
NG_011806.1:g.65579T>A , LRG_553:g.65579T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5664T>A MANE Select	ENSP00000356771.3:p.Val1888=
ENST00000367796.3:c.5679T>A	ENSP00000356770.3:p.Val1893=
ENST00000367797.7:c.5664T>A	ENSP00000356771.3:p.Val1888=
NM_000130.4:c.5664T>A , LRG_553t1:c.5664T>A	NP_000121.2:p.Val1888=
XM_017000660.2:c.5253T>A	XP_016856149.1:p.Val1751=
NM_000130.5:c.5664T>A MANE Select	NP_000121.2:p.Val1888=