Canonical Allele Identifier: CA343142055

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169541518T>C (hg19) ; chr1:g.169572280T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572280T>C , CM000663.2:g.169572280T>C	GRCh38
NC_000001.10:g.169541518T>C , CM000663.1:g.169541518T>C	GRCh37
NC_000001.9:g.167808142T>C	NCBI36
NG_011806.1:g.19252A>G , LRG_553:g.19252A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.314A>G MANE Select	ENSP00000356771.3:p.Lys105Arg
ENST00000367796.3:c.314A>G	ENSP00000356770.3:p.Lys105Arg
ENST00000367797.7:c.314A>G	ENSP00000356771.3:p.Lys105Arg
NM_000130.4:c.314A>G , LRG_553t1:c.314A>G	NP_000121.2:p.Lys105Arg
XM_017000660.2:c.-98A>G	XP_016856149.1:n.-98A>G
NM_000130.5:c.314A>G MANE Select	NP_000121.2:p.Lys105Arg