Canonical Allele Identifier: CA343142133

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169541539A>G (hg19) ; chr1:g.169572301A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572301A>G , CM000663.2:g.169572301A>G	GRCh38
NC_000001.10:g.169541539A>G , CM000663.1:g.169541539A>G	GRCh37
NC_000001.9:g.167808163A>G	NCBI36
NG_011806.1:g.19231T>C , LRG_553:g.19231T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.293T>C MANE Select	ENSP00000356771.3:p.Ile98Thr
ENST00000367796.3:c.293T>C	ENSP00000356770.3:p.Ile98Thr
ENST00000367797.7:c.293T>C	ENSP00000356771.3:p.Ile98Thr
NM_000130.4:c.293T>C , LRG_553t1:c.293T>C	NP_000121.2:p.Ile98Thr
XM_017000660.2:c.-119T>C	XP_016856149.1:n.-119T>C
NM_000130.5:c.293T>C MANE Select	NP_000121.2:p.Ile98Thr