Canonical Allele Identifier: CA2466815662

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863175G= , CM000685.2:g.154863175G=	GRCh38
NC_000023.10:g.154091450G= , CM000685.1:g.154091450G=	GRCh37
NC_000023.9:g.153744644G=	NCBI36
NG_011403.1:g.164549C=
NG_011403.2:g.164549C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6482C= MANE Select	ENSP00000353393.4:p.Pro2161=
ENST00000644698.1:c.215C=	ENSP00000495706.1:p.Pro72=
ENST00000330287.10:c.77C=	ENSP00000327895.6:p.Pro26=
ENST00000360256.8:c.6482C=	ENSP00000353393.4:p.Pro2161=
NM_000132.3:c.6482C=	NP_000123.1:p.Pro2161=
NM_019863.2:c.77C=	NP_063916.1:p.Pro26=
XM_011531126.1:c.6377C=	XP_011529428.1:p.Pro2126=
NM_000132.4:c.6482C= MANE Select	NP_000123.1:p.Pro2161=
NM_019863.3:c.77C=	NP_063916.1:p.Pro26=