Canonical Allele Identifier: CA421735117

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169495188T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169525950T>C , CM000663.2:g.169525950T>C	GRCh38
NC_000001.10:g.169495188T>C , CM000663.1:g.169495188T>C	GRCh37
NC_000001.9:g.167761812T>C	NCBI36
NG_011806.1:g.65582A>G , LRG_553:g.65582A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5667A>G MANE Select	ENSP00000356771.3:p.Gly1889=
ENST00000367796.3:c.5682A>G	ENSP00000356770.3:p.Gly1894=
ENST00000367797.7:c.5667A>G	ENSP00000356771.3:p.Gly1889=
NM_000130.4:c.5667A>G , LRG_553t1:c.5667A>G	NP_000121.2:p.Gly1889=
XM_017000660.2:c.5256A>G	XP_016856149.1:p.Gly1752=
NM_000130.5:c.5667A>G MANE Select	NP_000121.2:p.Gly1889=