Canonical Allele Identifier: CA2466807458

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837721G= , CM000685.2:g.154837721G=	GRCh38
NC_000023.10:g.154065996G= , CM000685.1:g.154065996G=	GRCh37
NC_000023.9:g.153719190G=	NCBI36
NG_011403.1:g.190003C=
NG_033065.1:g.1942C=
NG_011403.2:g.190003C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6932C= MANE Select	ENSP00000353393.4:p.Pro2311=
ENST00000644698.1:c.665C=	ENSP00000495706.1:p.Pro222=
ENST00000330287.10:c.527C=	ENSP00000327895.6:p.Pro176=
ENST00000360256.8:c.6932C=	ENSP00000353393.4:p.Pro2311=
NM_000132.3:c.6932C=	NP_000123.1:p.Pro2311=
NM_019863.2:c.527C=	NP_063916.1:p.Pro176=
XM_011531126.1:c.6827C=	XP_011529428.1:p.Pro2276=
NM_000132.4:c.6932C= MANE Select	NP_000123.1:p.Pro2311=
NM_019863.3:c.527C=	NP_063916.1:p.Pro176=