Canonical Allele Identifier: CA1206136772
Gene: F5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169532399T= , CM000663.2:g.169532399T= GRCh38
NC_000001.10:g.169501637T= , CM000663.1:g.169501637T= GRCh37
NC_000001.9:g.167768261T= NCBI36
NG_011806.1:g.59133A= , LRG_553:g.59133A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.4972-1377A= MANE Select ENSP00000356771.3:n.4972-1377A=
ENST00000367796.3:c.4987-1377A= ENSP00000356770.3:n.4987-1377A=
ENST00000367797.7:c.4972-1377A= ENSP00000356771.3:n.4972-1377A=
NM_000130.4:c.4972-1377A= , LRG_553t1:c.4972-1377A= NP_000121.2:n.4972-1377A=
XM_017000660.2:c.4561-1377A= XP_016856149.1:n.4561-1377A=
NM_000130.5:c.4972-1377A= MANE Select NP_000121.2:n.4972-1377A=
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