Canonical Allele Identifier: CA2466807435

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837669G= , CM000685.2:g.154837669G=	GRCh38
NC_000023.10:g.154065944G= , CM000685.1:g.154065944G=	GRCh37
NC_000023.9:g.153719138G=	NCBI36
NG_011403.1:g.190055C=
NG_033065.1:g.1994C=
NG_011403.2:g.190055C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6984C= MANE Select	ENSP00000353393.4:p.His2328=
ENST00000644698.1:c.717C=	ENSP00000495706.1:p.His239=
ENST00000330287.10:c.579C=	ENSP00000327895.6:p.His193=
ENST00000360256.8:c.6984C=	ENSP00000353393.4:p.His2328=
NM_000132.3:c.6984C=	NP_000123.1:p.His2328=
NM_019863.2:c.579C=	NP_063916.1:p.His193=
XM_011531126.1:c.6879C=	XP_011529428.1:p.His2293=
NM_000132.4:c.6984C= MANE Select	NP_000123.1:p.His2328=
NM_019863.3:c.579C=	NP_063916.1:p.His193=