Canonical Allele Identifier: CA1206144029

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169549627G= , CM000663.2:g.169549627G=	GRCh38
NC_000001.10:g.169518865G= , CM000663.1:g.169518865G=	GRCh37
NC_000001.9:g.167785489G=	NCBI36
NG_011806.1:g.41905C= , LRG_553:g.41905C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.1611+174C= MANE Select	ENSP00000356771.3:n.1611+174C=
ENST00000367796.3:c.1611+174C=	ENSP00000356770.3:n.1611+174C=
ENST00000367797.7:c.1611+174C=	ENSP00000356771.3:n.1611+174C=
NM_000130.4:c.1611+174C= , LRG_553t1:c.1611+174C=	NP_000121.2:n.1611+174C=
XM_017000660.2:c.1200+174C=	XP_016856149.1:n.1200+174C=
NM_000130.5:c.1611+174C= MANE Select	NP_000121.2:n.1611+174C=