Canonical Allele Identifier: CA2466807426

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837647T= , CM000685.2:g.154837647T=	GRCh38
NC_000023.10:g.154065922T= , CM000685.1:g.154065922T=	GRCh37
NC_000023.9:g.153719116T=	NCBI36
NG_011403.1:g.190077A=
NG_033065.1:g.2016A=
NG_011403.2:g.190077A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7006A= MANE Select	ENSP00000353393.4:p.Ile2336=
ENST00000644698.1:c.739A=	ENSP00000495706.1:p.Ile247=
ENST00000330287.10:c.601A=	ENSP00000327895.6:p.Ile201=
ENST00000360256.8:c.7006A=	ENSP00000353393.4:p.Ile2336=
NM_000132.3:c.7006A=	NP_000123.1:p.Ile2336=
NM_019863.2:c.601A=	NP_063916.1:p.Ile201=
XM_011531126.1:c.6901A=	XP_011529428.1:p.Ile2301=
NM_000132.4:c.7006A= MANE Select	NP_000123.1:p.Ile2336=
NM_019863.3:c.601A=	NP_063916.1:p.Ile201=