Canonical Allele Identifier: CA1206148576
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572212T= , CM000663.2:g.169572212T= GRCh38
NC_000001.10:g.169541450T= , CM000663.1:g.169541450T= GRCh37
NC_000001.9:g.167808074T= NCBI36
NG_011806.1:g.19320A= , LRG_553:g.19320A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.373+9A= MANE Select ENSP00000356771.3:n.373+9A=
ENST00000367796.3:c.373+9A= ENSP00000356770.3:n.373+9A=
ENST00000367797.7:c.373+9A= ENSP00000356771.3:n.373+9A=
NM_000130.4:c.373+9A= , LRG_553t1:c.373+9A= NP_000121.2:n.373+9A=
XM_017000660.2:c.-39+9A= XP_016856149.1:n.-39+9A=
NM_000130.5:c.373+9A= MANE Select NP_000121.2:n.373+9A=