Canonical Allele Identifier: CA1206133690
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525954A= , CM000663.2:g.169525954A= GRCh38
NC_000001.10:g.169495192A= , CM000663.1:g.169495192A= GRCh37
NC_000001.9:g.167761816A= NCBI36
NG_011806.1:g.65578T= , LRG_553:g.65578T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5663T= MANE Select ENSP00000356771.3:p.Val1888=
ENST00000367796.3:c.5678T= ENSP00000356770.3:p.Val1893=
ENST00000367797.7:c.5663T= ENSP00000356771.3:p.Val1888=
NM_000130.4:c.5663T= , LRG_553t1:c.5663T= NP_000121.2:p.Val1888=
XM_017000660.2:c.5252T= XP_016856149.1:p.Val1751=
NM_000130.5:c.5663T= MANE Select NP_000121.2:p.Val1888=