Canonical Allele Identifier: CA2466815674

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863204T= , CM000685.2:g.154863204T=	GRCh38
NC_000023.10:g.154091479T= , CM000685.1:g.154091479T=	GRCh37
NC_000023.9:g.153744673T=	NCBI36
NG_011403.1:g.164520A=
NG_011403.2:g.164520A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6453A= MANE Select	ENSP00000353393.4:p.Ser2151=
ENST00000644698.1:c.186A=	ENSP00000495706.1:p.Ser62=
ENST00000330287.10:c.48A=	ENSP00000327895.6:p.Ser16=
ENST00000360256.8:c.6453A=	ENSP00000353393.4:p.Ser2151=
NM_000132.3:c.6453A=	NP_000123.1:p.Ser2151=
NM_019863.2:c.48A=	NP_063916.1:p.Ser16=
XM_011531126.1:c.6348A=	XP_011529428.1:p.Ser2116=
NM_000132.4:c.6453A= MANE Select	NP_000123.1:p.Ser2151=
NM_019863.3:c.48A=	NP_063916.1:p.Ser16=