Canonical Allele Identifier: CA1206132471
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541826A= , CM000663.2:g.169541826A= GRCh38
NC_000001.10:g.169511064A= , CM000663.1:g.169511064A= GRCh37
NC_000001.9:g.167777688A= NCBI36
NG_011806.1:g.49706T= , LRG_553:g.49706T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.3264T= MANE Select ENSP00000356771.3:p.Ser1088=
ENST00000367796.3:c.3279T= ENSP00000356770.3:p.Ser1093=
ENST00000367797.7:c.3264T= ENSP00000356771.3:p.Ser1088=
NM_000130.4:c.3264T= , LRG_553t1:c.3264T= NP_000121.2:p.Ser1088=
XM_017000660.2:c.2853T= XP_016856149.1:p.Ser951=
NM_000130.5:c.3264T= MANE Select NP_000121.2:p.Ser1088=