Canonical Allele Identifier: CA1206136792
Gene: F5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169532474A= , CM000663.2:g.169532474A= GRCh38
NC_000001.10:g.169501712A= , CM000663.1:g.169501712A= GRCh37
NC_000001.9:g.167768336A= NCBI36
NG_011806.1:g.59058T= , LRG_553:g.59058T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.4972-1452T= MANE Select ENSP00000356771.3:n.4972-1452T=
ENST00000367796.3:c.4987-1452T= ENSP00000356770.3:n.4987-1452T=
ENST00000367797.7:c.4972-1452T= ENSP00000356771.3:n.4972-1452T=
NM_000130.4:c.4972-1452T= , LRG_553t1:c.4972-1452T= NP_000121.2:n.4972-1452T=
XM_017000660.2:c.4561-1452T= XP_016856149.1:n.4561-1452T=
NM_000130.5:c.4972-1452T= MANE Select NP_000121.2:n.4972-1452T=
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