Canonical Allele Identifier: CA1234662

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572308C>G , CM000663.2:g.169572308C>G	GRCh38
NC_000001.10:g.169541546C>G , CM000663.1:g.169541546C>G	GRCh37
NC_000001.9:g.167808170C>G	NCBI36
NG_011806.1:g.19224G>C , LRG_553:g.19224G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000130.5:c.286G>C MANE Select	NP_000121.2:p.Asp96His
ENST00000367797.9:c.286G>C MANE Select	ENSP00000356771.3:p.Asp96His
NM_000130.4:c.286G>C , LRG_553t1:c.286G>C	NP_000121.2:p.Asp96His
ENST00000367796.3:c.286G>C	ENSP00000356770.3:p.Asp96His
ENST00000367797.7:c.286G>C	ENSP00000356771.3:p.Asp96His
XM_017000660.2:c.-126G>C	XP_016856149.1:n.-126G>C