Canonical Allele Identifier: CA1206133663
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525925T= , CM000663.2:g.169525925T= GRCh38
NC_000001.10:g.169495163T= , CM000663.1:g.169495163T= GRCh37
NC_000001.9:g.167761787T= NCBI36
NG_011806.1:g.65607A= , LRG_553:g.65607A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.5692A= MANE Select ENSP00000356771.3:p.Thr1898=
ENST00000367796.3:c.5707A= ENSP00000356770.3:p.Thr1903=
ENST00000367797.7:c.5692A= ENSP00000356771.3:p.Thr1898=
NM_000130.4:c.5692A= , LRG_553t1:c.5692A= NP_000121.2:p.Thr1898=
XM_017000660.2:c.5281A= XP_016856149.1:p.Thr1761=
NM_000130.5:c.5692A= MANE Select NP_000121.2:p.Thr1898=