Canonical Allele Identifier: CA1206136163
Gene: F5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169530638T= , CM000663.2:g.169530638T= GRCh38
NC_000001.10:g.169499876T= , CM000663.1:g.169499876T= GRCh37
NC_000001.9:g.167766500T= NCBI36
NG_011806.1:g.60894A= , LRG_553:g.60894A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.5208+148A= MANE Select ENSP00000356771.3:n.5208+148A=
ENST00000367796.3:c.5223+148A= ENSP00000356770.3:n.5223+148A=
ENST00000367797.7:c.5208+148A= ENSP00000356771.3:n.5208+148A=
NM_000130.4:c.5208+148A= , LRG_553t1:c.5208+148A= NP_000121.2:n.5208+148A=
XM_017000660.2:c.4797+148A= XP_016856149.1:n.4797+148A=
NM_000130.5:c.5208+148A= MANE Select NP_000121.2:n.5208+148A=
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