Canonical Allele Identifier: CA1206132313

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541654G= , CM000663.2:g.169541654G=	GRCh38
NC_000001.10:g.169510892G= , CM000663.1:g.169510892G=	GRCh37
NC_000001.9:g.167777516G=	NCBI36
NG_011806.1:g.49878C= , LRG_553:g.49878C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3436C= MANE Select	ENSP00000356771.3:p.His1146=
ENST00000367796.3:c.3451C=	ENSP00000356770.3:p.His1151=
ENST00000367797.7:c.3436C=	ENSP00000356771.3:p.His1146=
NM_000130.4:c.3436C= , LRG_553t1:c.3436C=	NP_000121.2:p.His1146=
XM_017000660.2:c.3025C=	XP_016856149.1:p.His1009=
NM_000130.5:c.3436C= MANE Select	NP_000121.2:p.His1146=