Canonical Allele Identifier: CA2466844318

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953904T= , CM000685.2:g.154953904T=	GRCh38
NC_000023.10:g.154182179T= , CM000685.1:g.154182179T=	GRCh37
NC_000023.9:g.153835373T=	NCBI36
NG_011403.1:g.73820A=
NG_011403.2:g.73820A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1891A= MANE Select	ENSP00000353393.4:p.Asn631=
ENST00000647125.1:c.*1767A=	ENSP00000496062.1:n.*1767A=
ENST00000360256.8:c.1891A=	ENSP00000353393.4:p.Asn631=
NM_000132.3:c.1891A=	NP_000123.1:p.Asn631=
XM_011531126.1:c.1786A=	XP_011529428.1:p.Asn596=
NM_000132.4:c.1891A= MANE Select	NP_000123.1:p.Asn631=