Canonical Allele Identifier: CA1206136791
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169532468C= , CM000663.2:g.169532468C= GRCh38
NC_000001.10:g.169501706C= , CM000663.1:g.169501706C= GRCh37
NC_000001.9:g.167768330C= NCBI36
NG_011806.1:g.59064G= , LRG_553:g.59064G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.4972-1446G= MANE Select ENSP00000356771.3:n.4972-1446G=
ENST00000367796.3:c.4987-1446G= ENSP00000356770.3:n.4987-1446G=
ENST00000367797.7:c.4972-1446G= ENSP00000356771.3:n.4972-1446G=
NM_000130.4:c.4972-1446G= , LRG_553t1:c.4972-1446G= NP_000121.2:n.4972-1446G=
XM_017000660.2:c.4561-1446G= XP_016856149.1:n.4561-1446G=
NM_000130.5:c.4972-1446G= MANE Select NP_000121.2:n.4972-1446G=