Canonical Allele Identifier: CA2466814951

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860390T= , CM000685.2:g.154860390T=	GRCh38
NC_000023.10:g.154088665T= , CM000685.1:g.154088665T=	GRCh37
NC_000023.9:g.153741859T=	NCBI36
NG_011403.1:g.167334A=
NG_011403.2:g.167334A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+42A= MANE Select	ENSP00000353393.4:n.6900+42A=
ENST00000644698.1:c.633+42A=	ENSP00000495706.1:n.633+42A=
ENST00000330287.10:c.495+42A=	ENSP00000327895.6:n.495+42A=
ENST00000360256.8:c.6900+42A=	ENSP00000353393.4:n.6900+42A=
NM_000132.3:c.6900+42A=	NP_000123.1:n.6900+42A=
NM_019863.2:c.495+42A=	NP_063916.1:n.495+42A=
XM_011531126.1:c.6795+42A=	XP_011529428.1:n.6795+42A=
NM_000132.4:c.6900+42A= MANE Select	NP_000123.1:n.6900+42A=
NM_019863.3:c.495+42A=	NP_063916.1:n.495+42A=