Canonical Allele Identifier: CA2466842534

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154947764A= , CM000685.2:g.154947764A=	GRCh38
NC_000023.10:g.154176039A= , CM000685.1:g.154176039A=	GRCh37
NC_000023.9:g.153829233A=	NCBI36
NG_011403.1:g.79960T=
NG_011403.2:g.79960T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.2047T= MANE Select	ENSP00000353393.4:p.Tyr683=
ENST00000647125.1:c.*1779+6128T=	ENSP00000496062.1:n.*1779+6128T=
ENST00000360256.8:c.2047T=	ENSP00000353393.4:p.Tyr683=
NM_000132.3:c.2047T=	NP_000123.1:p.Tyr683=
XM_011531126.1:c.1942T=	XP_011529428.1:p.Tyr648=
NM_000132.4:c.2047T= MANE Select	NP_000123.1:p.Tyr683=