Canonical Allele Identifier: CA2466807427

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837652T= , CM000685.2:g.154837652T=	GRCh38
NC_000023.10:g.154065927T= , CM000685.1:g.154065927T=	GRCh37
NC_000023.9:g.153719121T=	NCBI36
NG_011403.1:g.190072A=
NG_033065.1:g.2011A=
NG_011403.2:g.190072A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7001A= MANE Select	ENSP00000353393.4:p.His2334=
ENST00000644698.1:c.734A=	ENSP00000495706.1:p.His245=
ENST00000330287.10:c.596A=	ENSP00000327895.6:p.His199=
ENST00000360256.8:c.7001A=	ENSP00000353393.4:p.His2334=
NM_000132.3:c.7001A=	NP_000123.1:p.His2334=
NM_019863.2:c.596A=	NP_063916.1:p.His199=
XM_011531126.1:c.6896A=	XP_011529428.1:p.His2299=
NM_000132.4:c.7001A= MANE Select	NP_000123.1:p.His2334=
NM_019863.3:c.596A=	NP_063916.1:p.His199=