Canonical Allele Identifier: CA1206133698
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525961T= , CM000663.2:g.169525961T= GRCh38
NC_000001.10:g.169495199T= , CM000663.1:g.169495199T= GRCh37
NC_000001.9:g.167761823T= NCBI36
NG_011806.1:g.65571A= , LRG_553:g.65571A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5656A= MANE Select ENSP00000356771.3:p.Thr1886=
ENST00000367796.3:c.5671A= ENSP00000356770.3:p.Thr1891=
ENST00000367797.7:c.5656A= ENSP00000356771.3:p.Thr1886=
NM_000130.4:c.5656A= , LRG_553t1:c.5656A= NP_000121.2:p.Thr1886=
XM_017000660.2:c.5245A= XP_016856149.1:p.Thr1749=
NM_000130.5:c.5656A= MANE Select NP_000121.2:p.Thr1886=