Canonical Allele Identifier: CA1206136776
Gene: F5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169532409C= , CM000663.2:g.169532409C= GRCh38
NC_000001.10:g.169501647C= , CM000663.1:g.169501647C= GRCh37
NC_000001.9:g.167768271C= NCBI36
NG_011806.1:g.59123G= , LRG_553:g.59123G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.4972-1387G= MANE Select ENSP00000356771.3:n.4972-1387G=
ENST00000367796.3:c.4987-1387G= ENSP00000356770.3:n.4987-1387G=
ENST00000367797.7:c.4972-1387G= ENSP00000356771.3:n.4972-1387G=
NM_000130.4:c.4972-1387G= , LRG_553t1:c.4972-1387G= NP_000121.2:n.4972-1387G=
XM_017000660.2:c.4561-1387G= XP_016856149.1:n.4561-1387G=
NM_000130.5:c.4972-1387G= MANE Select NP_000121.2:n.4972-1387G=
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