Canonical Allele Identifier: CA1206147070
Gene: F5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552778A= , CM000663.2:g.169552778A= GRCh38
NC_000001.10:g.169522016A= , CM000663.1:g.169522016A= GRCh37
NC_000001.9:g.167788640A= NCBI36
NG_011806.1:g.38754T= , LRG_553:g.38754T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1119-44T= MANE Select ENSP00000356771.3:n.1119-44T=
ENST00000367796.3:c.1119-44T= ENSP00000356770.3:n.1119-44T=
ENST00000367797.7:c.1119-44T= ENSP00000356771.3:n.1119-44T=
NM_000130.4:c.1119-44T= , LRG_553t1:c.1119-44T= NP_000121.2:n.1119-44T=
XM_017000660.2:c.708-44T= XP_016856149.1:n.708-44T=
NM_000130.5:c.1119-44T= MANE Select NP_000121.2:n.1119-44T=
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