Canonical Allele Identifier: CA1233513

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529619T>C , CM000663.2:g.169529619T>C	GRCh38
NC_000001.10:g.169498857T>C , CM000663.1:g.169498857T>C	GRCh37
NC_000001.9:g.167765481T>C	NCBI36
NG_011806.1:g.61913A>G , LRG_553:g.61913A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000130.5:c.5408A>G MANE Select	NP_000121.2:p.His1803Arg
ENST00000367797.9:c.5408A>G MANE Select	ENSP00000356771.3:p.His1803Arg
NM_000130.4:c.5408A>G , LRG_553t1:c.5408A>G	NP_000121.2:p.His1803Arg
ENST00000367796.3:c.5423A>G	ENSP00000356770.3:p.His1808Arg
ENST00000367797.7:c.5408A>G	ENSP00000356771.3:p.His1803Arg
XM_017000660.2:c.4997A>G	XP_016856149.1:p.His1666Arg