Canonical Allele Identifier: CA1206133696
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525959T= , CM000663.2:g.169525959T= GRCh38
NC_000001.10:g.169495197T= , CM000663.1:g.169495197T= GRCh37
NC_000001.9:g.167761821T= NCBI36
NG_011806.1:g.65573A= , LRG_553:g.65573A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5658A= MANE Select ENSP00000356771.3:p.Thr1886=
ENST00000367796.3:c.5673A= ENSP00000356770.3:p.Thr1891=
ENST00000367797.7:c.5658A= ENSP00000356771.3:p.Thr1886=
NM_000130.4:c.5658A= , LRG_553t1:c.5658A= NP_000121.2:p.Thr1886=
XM_017000660.2:c.5247A= XP_016856149.1:p.Thr1749=
NM_000130.5:c.5658A= MANE Select NP_000121.2:p.Thr1886=