Canonical Allele Identifier: CA1146508896
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555156C= , CM000663.2:g.169555156C= GRCh38
NC_000001.10:g.169524394C= , CM000663.1:g.169524394C= GRCh37
NC_000001.9:g.167791018C= NCBI36
NG_011806.1:g.36376G= , LRG_553:g.36376G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1118+26G= MANE Select ENSP00000356771.3:n.1118+26G=
ENST00000367796.3:c.1118+26G= ENSP00000356770.3:n.1118+26G=
ENST00000367797.7:c.1118+26G= ENSP00000356771.3:n.1118+26G=
NM_000130.4:c.1118+26G= , LRG_553t1:c.1118+26G= NP_000121.2:n.1118+26G=
XM_017000660.2:c.707+26G= XP_016856149.1:n.707+26G=
NM_000130.5:c.1118+26G= MANE Select NP_000121.2:n.1118+26G=