Canonical Allele Identifier: CA1206148869
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572550A= , CM000663.2:g.169572550A= GRCh38
NC_000001.10:g.169541788A= , CM000663.1:g.169541788A= GRCh37
NC_000001.9:g.167808412A= NCBI36
NG_011806.1:g.18982T= , LRG_553:g.18982T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.251-207T= MANE Select ENSP00000356771.3:n.251-207T=
ENST00000367796.3:c.251-207T= ENSP00000356770.3:n.251-207T=
ENST00000367797.7:c.251-207T= ENSP00000356771.3:n.251-207T=
NM_000130.4:c.251-207T= , LRG_553t1:c.251-207T= NP_000121.2:n.251-207T=
XM_017000660.2:c.-161-207T= XP_016856149.1:n.-161-207T=
NM_000130.5:c.251-207T= MANE Select NP_000121.2:n.251-207T=