Canonical Allele Identifier: CA421735121

Gene: F5

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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